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Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination
Harel, Tamar, Quek, Debra Q. Y., Wong, Bernice H., Cazenave-Gassiot, Amaury, Wenk, Markus R., Fan, Hao, Berger, Itai, Shmueli, Dorit, Shaag, Avraham, Silver, David L., Elpeleg, Orly, Edvardson, ShimonLanguage:
english
Journal:
neurogenetics
DOI:
10.1007/s10048-018-0556-6
Date:
July, 2018
File:
PDF, 3.19 MB
english, 2018