Linkage of a gene for familial hypobetalipoproteinemia to chromosome 3p21.1-22.

Familial hypobetalipoproteinemia (FHBL) is an apparently autosomal dominant disorder of lipid metabolism characterized by less than fifth percentile age- and sex-specific levels of apolipoprotein beta (apobeta) and low-density lipoprotein-cholesterol. In a minority of cases, FHBL is due to truncatio...

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Bibliografiska uppgifter
Huvudupphovsmän: Yuan, B, Neuman, R, Duan, S H, Weber, J L, Kwok, P Y, Saccone, N L, Wu, J S, Liu, K Y, Schonfeld, G
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2000
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1378026/
https://ncbi.nlm.nih.gov/pubmed/10762553
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