A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family

BACKGROUND: Primary microcephaly (MCPH) is a rare developmental defect characterized by impaired cognitive functions, retarded neurodevelopment and reduced brain size. It is genetically heterogeneous and more than 17 genes so far have been identified that are associated with this disease. OBJECTIVE:...

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Detaylı Bibliyografya
Yayımlandı:Ann Saudi Med
Asıl Yazarlar: Naseer, Muhammad Imran, Rasool, Mahmood, Sogaty, Sameera, Chaudhary, Rukhaa Adeel, Mansour, Haifa Mansour, Chaudhary, Adeel G., Abuzenadah, Adel M., Al-Qahtani, Mohammad H.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: King Faisal Specialist Hospital and Research Centre 2017
Konular:
Original Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6150548/
https://ncbi.nlm.nih.gov/pubmed/28377545
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5144/0256-4947.2017.148
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