Multiplex ligation-dependent probe amplification analysis to screen for deletions and duplications of theLDLRgene in patients with familial hypercholesterolaemia-Reference-Cited by-同舟云学术

Multiplex ligation-dependent probe amplification analysis to screen for deletions and duplications of theLDLRgene in patients with familial hypercholesterolaemia

Published:2009-07 Issue:1 Volume:76 Page:69-75
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Taylor A,Martin B,Wang D,Patel K,Humphries SE,Norbury G

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2009.01168.x/fullpdf

Reference26 articles.

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2. Genetic heterogeneity of autosomal dominant hypercholesterolemia;Varret;Clin Genet,2008

3. Census of clinics providing specialist lipid services in the United Kingdom;Marks;J Public Health (Oxf),2004

4. Mechanisms of disease: genetic causes of familial hypercholesterolemia;Soutar;Nat Clin Pract Cardiovasc Med,2007

5. Update and analysis of the University College London low density lipoprotein receptor familial hypercholesterolemia database;Leigh;Ann Hum Genet,2008

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