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Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination

Overview of attention for article published in neurogenetics, July 2018
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Mentioned by

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2 X users
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2 patents

Citations

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44 Dimensions

Readers on

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37 Mendeley
Summary X Patents Dimensions citations
So far, Dimensions has found 44 publications that cite this research output.

44

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