KCNJ2 Mutation Results in Andersen Syndrome with Sex-Specific Cardiac and Skeletal Muscle Phenotypes
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference20 articles.
1. Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies: a new syndrome?;Andersen;Acta Paediat Scand,1971
2. Reduced penetrance, variable expressivity and genetic heterogeneity of familial atrial septal defect;Benson;Circulation,1998
3. Andersen syndrome autosomal dominant in three generations;Canun;Am J Med Genet,1999
4. Genetic and functional linkage of Kir5.1 and Kir2.1 channel subunits;Derst;FEBS Letters,2001
5. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches;Hamill;Pflugers Arch,1981
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