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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
PubMed
Abstract

No abstract available in PubMed .

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