A mutation in Ampd2 is associated with nephrotic syndrome and hypercholesterolemia in mice-Reference-Cited by-同舟云学术

A mutation in Ampd2 is associated with nephrotic syndrome and hypercholesterolemia in mice

Published:2014-10-31 Issue:1 Volume:13 Page:
ISSN:1476-511X
Container-title:Lipids in Health and Disease
language:en
Short-container-title:Lipids Health Dis

Author:

Helmering Joan,Juan Todd,Li Chi Ming,Chhoa Mark,Baron Will,Gyuris Tibor,Richards William G,Turk James R,Lawrence Jeff,Cosgrove Patrick A,Busby Jim,Kim Ki Won,Kaufman Stephen A,Cummings Connie,Carlson George,Véniant Murielle M,Lloyd David J

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://link.springer.com/content/pdf/10.1186/1476-511X-13-167.pdf

Reference31 articles.

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3. Abifadel M, Varret M, Rabes JP, Allard D, Ouguerram K, Devillers M, Cruaud C, Benjannet S, Wickham L, Erlich D, Derré A, Villéger L, Farnier M, Beucler I, Bruckert E, Chambaz J, Chanu B, Lecerf JM, Luc G, Moulin P, Weissenbach J, Prat A, Krempf M, Junien C, Seidah NG, Boileau C: Mutations in PCSK9 cause autosomal dominant hypercholesterolemia. Nat Genet. 2003, 34: 154-156. 10.1038/ng1161

4. Tybjaerg-Hansen A, Steffensen R, Meinertz H, Schnohr P, Nordestgaard BG: Association of mutations in the apolipoprotein B gene with hypercholesterolemia and the risk of ischemic heart disease. N Engl J Med. 1998, 338: 1577-1584. 10.1056/NEJM199805283382203

5. Soutar AK, Naoumova RP: Mechanisms of disease: genetic causes of familial hypercholesterolemia. Nat Clin Pract Cardiovasc Med. 2007, 4: 214-225. 10.1038/ncpcardio0836

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