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Two novel LDL receptor mutations in familial hypercholesterolemia: C122Y and E296X
J Genschel1, H P Thomas, U Kassner
1Campus Charité Mitte, Med. Klinik m.S. Gastroenterologie, Hepatologie und Endokrinologie, Berlin, Germany. janine.genschel@charite.de
Human Mutation
|April 11, 2001
Abstract
No abstract available in PubMed .
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