Mutation detection rate and spectrum in familial hypercholesterolaemia patients in the UK pilot cascade project-Reference-Cited by-同舟云学术

Mutation detection rate and spectrum in familial hypercholesterolaemia patients in the UK pilot cascade project

Published:2009-12-02 Issue:6 Volume:77 Page:572-580
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Taylor A,Wang D,Patel K,Whittall R,Wood G,Farrer M,Neely RDG,Fairgrieve S,Nair D,Barbir M,Jones JL,Egan S,Everdale R,Lolin Y,Hughes E,Cooper JA,Hadfield SG,Norbury G,Humphries SE

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2009.01356.x/fullpdf

Reference44 articles.

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4. Reductions in all-cause, cancer, and coronary mortality in statin-treated patients with heterozygous familial hypercholesterolaemia: a prospective registry study;Neil;Eur Heart J,2008

5. Efficacy of statins in familial hypercholesterolaemia: a long term cohort study;Versmissen;BMJ,2008

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