Correction to: Expanding the genetic heterogeneity of intellectual disability

Shams Anazi¹, Sateesh Maddirevula¹, Vincenzo Salpietro², Yasmine T Asi³, Saud Alsahli¹, Amal Alhashem⁴, Hanan E Shamseldin¹, Fatema AlZahrani¹, Nisha Patel¹, Niema Ibrahim¹, Firdous M Abdulwahab¹, Mais Hashem¹, Nadia Alhashmi⁵, Fathiya Al Murshedi⁵, Adila Al Kindy⁵, Ahmad Alshaer⁶, Ahmed Rumayyan^{7

8}, Saeed Al Tala⁹, Wesam Kurdi¹⁰, Abdulaziz Alsaman¹¹, Ali Alasmari¹¹, Selina Banu¹², Tipu Sultan¹³, Mohammed M Saleh¹¹, Hisham Alkuraya¹⁴, Mustafa A Salih¹⁵, Hesham Aldhalaan⁶, Tawfeg Ben-Omran¹⁶, Fatima Al Musafri¹⁶, Rehab Ali¹⁶, Jehan Suleiman¹⁷, Brahim Tabarki⁴, Ayman W El-Hattab¹⁸, Caleb Bupp¹⁹, Majid Alfadhel²⁰, Nada Al Tassan^{1

21}, Dorota Monies^{1

21}, Stefan T Arold²², Mohamed Abouelhoda^{1

21}, Tammaryn Lashley³, Henry Houlden², Eissa Faqeih¹¹, Fowzan S Alkuraya^{23

24

25

26

27}

Affiliations

¹ Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
² Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
³ Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of Neurology, University College London, London, UK.
⁴ Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
⁵ Department of Genetics, College of Medicine, Sultan Qaboos University, Muscat, Sultanate of Oman.
⁶ Pediatric Neurology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
⁷ King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
⁸ Neurology Division, Department of Pediatrics, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
⁹ Department of Pediatrics and Genetic Unit, Armed Forces Hospital Khamis Mushayt, Riyadh, Saudi Arabia.
¹⁰ Department of Obstetrics and Gynecology, King Faisal Specialist Hospital, Riyadh, Saudi Arabia.
¹¹ Department of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
¹² Department of Pediatric Neurology, ICH and SSF Hospital Mirpur, Dhaka, 1216, Bangladesh.
¹³ Department of Pediatric Neurology, Institute of Child Health and The Children's Hospital Lahore, 381-D/2, Lahore, Pakistan.
¹⁴ Department of Ophthalmology, Specialized Medical Center Hospital, Riyadh, Saudi Arabia.
¹⁵ Division of Pediatric Neurology, Department of Pediatrics, King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia.
¹⁶ Clinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
¹⁷ Division of Neurology, Department of Pediatrics, Tawam Hospital, Al Ain, United Arab Emirates.
¹⁸ Division of Clinical Genetics and Metabolic Disorders, Department of Pediatrics, Tawam Hospital, Al-Ain, United Arab Emirates.
¹⁹ Spectrum Health Genetics, Grand Rapids, MI, USA.
²⁰ Genetics Division, Department of Pediatrics, King Abdullah International Medical Research Centre, King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
²¹ Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
²² Division of Biological and Environmental Sciences and Engineering (BESE), Computational Bioscience Research Center (CBRC), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
²³ Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. falkuraya@kfshrc.edu.sa.
²⁴ Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia. falkuraya@kfshrc.edu.sa.
²⁵ Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia. falkuraya@kfshrc.edu.sa.
²⁶ Spectrum Health Genetics, Grand Rapids, MI, USA. falkuraya@kfshrc.edu.sa.
²⁷ Division of Biological and Environmental Sciences and Engineering (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia. falkuraya@kfshrc.edu.sa.

PMID: 29288388
DOI: 10.1007/s00439-017-1859-7

Published Erratum

Correction to: Expanding the genetic heterogeneity of intellectual disability

Shams Anazi et al. Hum Genet. 2018 Jan.

. 2018 Jan;137(1):105-109.

doi: 10.1007/s00439-017-1859-7.

Authors

Affiliations

¹ Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
² Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
³ Queen Square Brain Bank for Neurological Disorders, Department of Molecular Neuroscience, UCL Institute of Neurology, University College London, London, UK.
⁴ Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
⁵ Department of Genetics, College of Medicine, Sultan Qaboos University, Muscat, Sultanate of Oman.
⁶ Pediatric Neurology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
⁷ King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
⁸ Neurology Division, Department of Pediatrics, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
⁹ Department of Pediatrics and Genetic Unit, Armed Forces Hospital Khamis Mushayt, Riyadh, Saudi Arabia.
¹⁰ Department of Obstetrics and Gynecology, King Faisal Specialist Hospital, Riyadh, Saudi Arabia.
¹¹ Department of Pediatric Subspecialties, Children's Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.
¹² Department of Pediatric Neurology, ICH and SSF Hospital Mirpur, Dhaka, 1216, Bangladesh.
¹³ Department of Pediatric Neurology, Institute of Child Health and The Children's Hospital Lahore, 381-D/2, Lahore, Pakistan.
¹⁴ Department of Ophthalmology, Specialized Medical Center Hospital, Riyadh, Saudi Arabia.
¹⁵ Division of Pediatric Neurology, Department of Pediatrics, King Khalid University Hospital and College of Medicine, King Saud University, Riyadh, Saudi Arabia.
¹⁶ Clinical and Metabolic Genetics, Department of Pediatrics, Hamad Medical Corporation, Doha, Qatar.
¹⁷ Division of Neurology, Department of Pediatrics, Tawam Hospital, Al Ain, United Arab Emirates.
¹⁸ Division of Clinical Genetics and Metabolic Disorders, Department of Pediatrics, Tawam Hospital, Al-Ain, United Arab Emirates.
¹⁹ Spectrum Health Genetics, Grand Rapids, MI, USA.
²⁰ Genetics Division, Department of Pediatrics, King Abdullah International Medical Research Centre, King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
²¹ Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
²² Division of Biological and Environmental Sciences and Engineering (BESE), Computational Bioscience Research Center (CBRC), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
²³ Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. falkuraya@kfshrc.edu.sa.
²⁴ Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia. falkuraya@kfshrc.edu.sa.
²⁵ Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia. falkuraya@kfshrc.edu.sa.
²⁶ Spectrum Health Genetics, Grand Rapids, MI, USA. falkuraya@kfshrc.edu.sa.
²⁷ Division of Biological and Environmental Sciences and Engineering (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia. falkuraya@kfshrc.edu.sa.

PMID: 29288388
DOI: 10.1007/s00439-017-1859-7

Abstract

Variant nomenclature discrepancy was identified in the article.

PubMed Disclaimer

Erratum for

Expanding the genetic heterogeneity of intellectual disability.
Anazi S, Maddirevula S, Salpietro V, Asi YT, Alsahli S, Alhashem A, Shamseldin HE, AlZahrani F, Patel N, Ibrahim N, Abdulwahab FM, Hashem M, Alhashmi N, Al Murshedi F, Al Kindy A, Alshaer A, Rumayyan A, Al Tala S, Kurdi W, Alsaman A, Alasmari A, Banu S, Sultan T, Saleh MM, Alkuraya H, Salih MA, Aldhalaan H, Ben-Omran T, Al Musafri F, Ali R, Suleiman J, Tabarki B, El-Hattab AW, Bupp C, Alfadhel M, Al Tassan N, Monies D, Arold ST, Abouelhoda M, Lashley T, Houlden H, Faqeih E, Alkuraya FS. Anazi S, et al. Hum Genet. 2017 Nov;136(11-12):1419-1429. doi: 10.1007/s00439-017-1843-2. Epub 2017 Sep 22. Hum Genet. 2017. PMID: 28940097

Publication types

Actions

LinkOut - more resources

Full Text Sources
- Springer
Other Literature Sources
- scite Smart Citations
Molecular Biology Databases
- GlyGen glycoinformatics resource

Save citation to file

Email citation

Add to Collections

Add to My Bibliography

Your saved search

Create a file for external citation management software

Your RSS Feed

Correction to: Expanding the genetic heterogeneity of intellectual disability

Affiliations

Correction to: Expanding the genetic heterogeneity of intellectual disability

Authors

Affiliations

Abstract

Erratum for

Publication types

LinkOut - more resources

Full Text Sources

Other Literature Sources

Molecular Biology Databases