Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndrome

• المؤلفون الرئيسيون: Guemez-Gamboa, Alicia, Nguyen, Long N, Yang, Hongbo, Zaki, Maha S, Kara, Majdi, Ben-Omran, Tawfeg, Akizu, Naiara, Rosti, Rasim Ozgur, Rosti, Basak, Scott, Eric, Schroth, Jana, Copeland, Brett, Vaux, Keith K, Cazenave-Gassiot, Amaury, Quek, Debra QY, Wong, Bernice H, Tan, Bryan C, Wenk, Markus R, Gunel, Murat, Gabriel, Stacey, Chi, Neil C, Silver, David L, Gleeson, Joseph G
• مؤلفون آخرون: DUKE-NUS MEDICAL SCHOOL
• التنسيق: مقال
• اللغة: English
• منشور في: NATURE PUBLISHING GROUP 2020
• الموضوعات: Science & Technology; Life Sciences & Biomedicine; Genetics & Heredity; FATTY-ACID COMPOSITION; DOCOSAHEXAENOIC ACID; BARRIER; PERICYTES; NEUROGENESIS; EXPRESSION; DISCOVERY; MOUSE
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/170831
• المؤسسة: National University of Singapore

10.1038/ng.3311