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Analysis of the frequency and spectrum of mutations recognised to cause familial hypercholesterolaemia in routine clinical practice in a UK specialist hospital lipid clinic

✍ Scribed by Futema, Marta; Whittall, Ros A.; Kiley, Amy; Steel, Louisa K.; Cooper, Jackie A.; Badmus, Ebele; Leigh, Sarah E.; Karpe, Fredrik; Neil, H. Andrew W.; Humphries, Steve E.

Book ID: 122203707
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 767 KB
Volume: 229
Category: Article
ISSN: 0021-9150
DOI: 10.1016/j.atherosclerosis.2013.04.011

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