Co-segregation of elevated LDL with a novel mutation (D92K) of the LDL receptor in a kindred with multiple lipoprotein abnormalities-Reference-Cited by-同舟云学术

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Co-segregation of elevated LDL with a novel mutation (D92K) of the LDL receptor in a kindred with multiple lipoprotein abnormalities

Published:2000-05 Issue:3 Volume:45 Page:154-158
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Wu L. L.,Hopkins P. N.,Xin Y.,Stephenson S. H.,Williams R. R.,Nobe Y.,Kajita M.,Nakajima T.,Emi M.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/jhg200033.pdf

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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2. Combined hyperlipidemia;Current Opinion in Lipidology;2016-04

3. Contribution of mutations in low density lipoprotein receptor (LDLR) and lipoprotein lipase (LPL) genes to familial combined hyperlipidemia (FCHL): A reappraisal by using a resequencing approach;Atherosclerosis;2015-10

4. Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East;Orphanet Journal of Rare Diseases;2012-08-21

5. Familial Hypercholesterolemias: Prevalence, genetics, diagnosis and screening recommendations from the National Lipid Association Expert Panel on Familial Hypercholesterolemia;Journal of Clinical Lipidology;2011-06

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