Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination
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| Description | scientific article published on 24 July 2018 |
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author: Itai Berger Tamar Harel Markus R. Wenk Amaury Cazenave-Gassiot |
| Publication date | July 24, 2018 |
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