A partially inactivating mutation in the sodium-dependent lysophosphatidylcholine transporter MFSD2A causes a non-lethal microcephaly syndrome

• المؤلفون الرئيسيون: Alakbarzade, Vafa, Hameed, Abdul, Quek, Debra QY, Chioza, Barry A, Baple, Emma L, Cazenave-Gassiot, Amaury, Nguyen, Long N, Wenk, Markus R, Ahmad, Arshia Q, Sreekantan-Nair, Ajith, Weedon, Michael N, Rich, Phil, Patton, Michael A, Warner, Thomas T, Silver, David L, Crosby, Andrew H
• مؤلفون آخرون: BIOCHEMISTRY
• التنسيق: مقال
• اللغة: English
• منشور في: NATURE PUBLISHING GROUP 2020
• الموضوعات: Science & Technology; Life Sciences & Biomedicine; Genetics & Heredity; RAT
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/170830
• المؤسسة: National University of Singapore

10.1038/ng.3313