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Genetic diagnosis of familial hypercholesterolaemia: a mutation and a rare non-pathogenic amino acid variant in the same family

✍ Scribed by Rossitza P Naoumova; Clare Neuwirth; Bruce Pottinger; Ros Whittal; Stephen E Humphries; Anne K Soutar

Book ID: 118420267
Publisher: Elsevier Science
Year: 2004
Tongue: English
Weight: 124 KB
Volume: 174
Category: Article
ISSN: 0021-9150
DOI: 10.1016/j.atherosclerosis.2004.01.001

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