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Article

A novel mutation of apolipoprotein B in a French Canadian family with homozygous hypobetalipoproteinemia.

Journal of clinical lipidology - 1 Jan 2000

Gangloff Anne, Bergeron Jean, Couture Patrick, Martins Rebecca, Hegele Robert A, Gagné Claude

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Share to Apolipoproteins B
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 21981844
DOI: 10.1016/j.jacl.2011.06.014

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A novel mutation of apolipoprotein B in a French Canadian family with homozygous hypobetalipoproteinemia.PMID 21981844Read ↗

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