Human cholesterol 7α-hydroxylase (CYP7A1) deficiency has a hypercholesterolemic phenotype-Reference-Cited by-同舟云学术

Human cholesterol 7α-hydroxylase (CYP7A1) deficiency has a hypercholesterolemic phenotype

Published:2002-07-01 Issue:1 Volume:110 Page:109-117
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Pullinger Clive R.,Eng Celeste,Salen Gerald,Shefer Sarah,Batta Ashok K.,Erickson Sandra K.,Verhagen Andrea,Rivera Christopher R.,Mulvihill Sean J.,Malloy Mary J.,Kane John P.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference58 articles.

1. The Cholesterol Quartet

2. Autosomal Recessive Hypercholesterolemia Caused by Mutations in a Putative LDL Receptor Adaptor Protein

3. Accumulation of Dietary Cholesterol in Sitosterolemia Caused by Mutations in Adjacent ABC Transporters

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