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Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination. https://t.co/OQFRYtTWWN
Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination. https://t.co/OQFRYtTWWN
BII scientists discover mutations linked with diseases like microcephaly and hypomyelination https://t.co/zdqMqCpn82