Abstract
Familial hypercholesterolemia is an autosomal dominant inherited condition characterized by a mutation in the low-density lipoprotein receptor (LDLR) gene. A database has been set up on the World Wide Web for mutations in the LDLR gene.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Base Sequence
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Databases as Topic
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Humans
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Hyperlipoproteinemia Type II / genetics*
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Medical Informatics*
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Molecular Sequence Data
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Mutation*
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Receptors, LDL / genetics*
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United States