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Comment

. 2016 Feb;79(2):335-7.

doi: 10.1002/ana.24591. Epub 2016 Jan 19.

A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's Disease

Liena Elbaghir Omer Elsayed^{1

2

3}, Valérie Drouet¹, Tatiana Usenko¹, Inaam N Mohammed³, Ahlam AbdAlrahman Ahmed Hamed³, Maha Abdelmoneim Elseed³, Mustafa A M Salih⁴, Mahmoud Eltayeb Koko⁵, Ashraf Yahia Osman Mohamed⁶, Rayan Abubaker Siddig⁷, Mustafa Idris Elbashir³, Muntaser Eltayeb Ibrahim⁵, Alexandra Durr^{1

8}, Giovanni Stevanin^{1

2

8}, Suzanne Lesage¹, Ammar Eltahir Ahmed³, Alexis Brice^{1

8}

Affiliations

Affiliations

¹ Inserm U1127, CNRS UMR7225, Sorbonne Universités, UPMC Université Paris 06, UMR_S1127, Institut du Cerveau et de la Moelle épinière, Paris, France.
² Ecole Pratique des Hautes Etudes, Pitié-Salpêtrière Hospital, ICM, Paris, France.
³ Faculty of Medicine, University of Khartoum, Khartoum, Sudan.
⁴ Division of Pediatric Neurology, Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
⁵ Department of Molecular Biology, Institute of Endemic Diseases, University of Khartoum, Khartoum, Sudan.
⁶ Department of Biochemistry, Faculty of Medicine, National University, Khartoum, Sudan.
⁷ Faculty of Science, University of Elneelen, Khartoum, Sudan.
⁸ APHP, Department of Genetics, Pitié-Salpêtrière Hospital, Paris, France.

PMID: 26703368
DOI: 10.1002/ana.24591

Comment

A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's Disease

Liena Elbaghir Omer Elsayed et al. Ann Neurol. 2016 Feb.

. 2016 Feb;79(2):335-7.

doi: 10.1002/ana.24591. Epub 2016 Jan 19.

Authors

Liena Elbaghir Omer Elsayed^{1

2

3}, Valérie Drouet¹, Tatiana Usenko¹, Inaam N Mohammed³, Ahlam AbdAlrahman Ahmed Hamed³, Maha Abdelmoneim Elseed³, Mustafa A M Salih⁴, Mahmoud Eltayeb Koko⁵, Ashraf Yahia Osman Mohamed⁶, Rayan Abubaker Siddig⁷, Mustafa Idris Elbashir³, Muntaser Eltayeb Ibrahim⁵, Alexandra Durr^{1

8}, Giovanni Stevanin^{1

2

8}, Suzanne Lesage¹, Ammar Eltahir Ahmed³, Alexis Brice^{1

8}

Affiliations

¹ Inserm U1127, CNRS UMR7225, Sorbonne Universités, UPMC Université Paris 06, UMR_S1127, Institut du Cerveau et de la Moelle épinière, Paris, France.
² Ecole Pratique des Hautes Etudes, Pitié-Salpêtrière Hospital, ICM, Paris, France.
³ Faculty of Medicine, University of Khartoum, Khartoum, Sudan.
⁴ Division of Pediatric Neurology, Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
⁵ Department of Molecular Biology, Institute of Endemic Diseases, University of Khartoum, Khartoum, Sudan.
⁶ Department of Biochemistry, Faculty of Medicine, National University, Khartoum, Sudan.
⁷ Faculty of Science, University of Elneelen, Khartoum, Sudan.
⁸ APHP, Department of Genetics, Pitié-Salpêtrière Hospital, Paris, France.

PMID: 26703368
DOI: 10.1002/ana.24591

No abstract available

PubMed Disclaimer

Comment in

Reply.
Olgiati S, Quadri M, Mandemakers W, Bonifati V. Olgiati S, et al. Ann Neurol. 2016 Feb;79(2):337-8. doi: 10.1002/ana.24587. Epub 2016 Jan 19. Ann Neurol. 2016. PMID: 26702604 No abstract available.

Comment on

DNAJC6 Mutations Associated With Early-Onset Parkinson's Disease.
Olgiati S, Quadri M, Fang M, Rood JP, Saute JA, Chien HF, Bouwkamp CG, Graafland J, Minneboo M, Breedveld GJ, Zhang J; International Parkinsonism Genetics Network; Verheijen FW, Boon AJ, Kievit AJ, Jardim LB, Mandemakers W, Barbosa ER, Rieder CR, Leenders KL, Wang J, Bonifati V. Olgiati S, et al. Ann Neurol. 2016 Feb;79(2):244-56. doi: 10.1002/ana.24553. Epub 2016 Jan 14. Ann Neurol. 2016. PMID: 26528954

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