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Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination
PaperCitations, authors & open-access status
Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 56 citations, 2018 year and closed oa status.
56
Citations
2018
Year
closed
OA Status