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Case Reports

. 2018 Dec;94(6):586-587.

doi: 10.1111/cge.13443. Epub 2018 Oct 11.

A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease

Hanadi A Abdelrahman¹, Aisha M Al-Shamsi², Bassam R Ali^{1

3}, Lihadh Al-Gazali¹

Affiliations

Affiliations

¹ College of Medicine and Heath Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.
² Paediatrics Department, Tawam Hospital, Al-Ain, United Arab Emirates.
³ Zayed Center for Health sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.

PMID: 30308082
DOI: 10.1111/cge.13443

Case Reports

A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease

Hanadi A Abdelrahman et al. Clin Genet. 2018 Dec.

. 2018 Dec;94(6):586-587.

doi: 10.1111/cge.13443. Epub 2018 Oct 11.

Authors

Hanadi A Abdelrahman¹, Aisha M Al-Shamsi², Bassam R Ali^{1

3}, Lihadh Al-Gazali¹

Affiliations

¹ College of Medicine and Heath Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.
² Paediatrics Department, Tawam Hospital, Al-Ain, United Arab Emirates.
³ Zayed Center for Health sciences, United Arab Emirates University, Al-Ain, United Arab Emirates.

PMID: 30308082
DOI: 10.1111/cge.13443

No abstract available

PubMed Disclaimer

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