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