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pubmed-article:20124734pubmed:abstractTextThe autosomal recessive hypercholesterolemia (ARH) gene is located on chromosome 1p35 and encodes a 308-amino acid protein containing a phosphotyrosine-binding domain. Several researchers have identified mutations of ARH that cause autosomal recessive hypercholesterolemia; however, it remains unknown whether this gene is involved in common hypercholesterolemia.lld:pubmed
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pubmed-article:20124734pubmed:articleTitleA novel Thr56Met mutation of the autosomal recessive hypercholesterolemia gene associated with hypercholesterolemia.lld:pubmed
pubmed-article:20124734pubmed:affiliationDepartment of Atherosclerosis and Diabetes, National Cardiovascular Center, Osaka, Japan.lld:pubmed
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