A Mutation in the Human Lipoprotein Lipase Gene as the Most Common Cause of Familial Chylomicronemia in French Canadians-Reference-Cited by-同舟云学术

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A Mutation in the Human Lipoprotein Lipase Gene as the Most Common Cause of Familial Chylomicronemia in French Canadians

Published:1991-06-20 Issue:25 Volume:324 Page:1761-1766
ISSN:0028-4793
Container-title:New England Journal of Medicine
language:en
Short-container-title:N Engl J Med

Author:

Ma Yuanhong,Henderson Howard E.,Ven Murthy M.R.,Roederer Ghislaine,Monsalve Maria V.,Clarke Lorne A.,Normand Thierry,Julien Pierre,Gagné Claude,Lambert Marie,Davignon Jean,Lupien Paul J.,Brunzell John,Hayden Michael R.

Publisher

Massachusetts Medical Society

Subject

General Medicine

Link

http://www.nejm.org/doi/pdf/10.1056/NEJM199106203242502

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3. Characterizing familial chylomicronemia syndrome: Baseline data of the APPROACH study;Journal of Clinical Lipidology;2018-09

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5. Identifying suspected familial chylomicronemia syndrome;Baylor University Medical Center Proceedings;2018-05-21

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