Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy

Published:2002-02-01 Issue:3 Volume:109 Page:357-362
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Arad Michael,Benson D. Woodrow,Perez-Atayde Antonio R.,McKenna William J.,Sparks Elizabeth A.,Kanter Ronald J.,McGarry Kate,Seidman J.G.,Seidman Christine E.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference28 articles.

1. Dealing with energy demand: the AMP-activated protein kinase

2. Mutations in the gamma2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

3. Identification of a Gene Responsible for Familial Wolff–Parkinson–White Syndrome

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