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[Same genotype and different phenotypes in a family with PRKAG2 gene mutation].

Authors
Type
Published Article
Journal
Zhonghua xin xue guan bing za zhi
Publication Date
Volume
35
Issue
6
Pages
552–554
Identifiers
PMID: 17711718
Source
Medline
License
Unknown

Abstract

Besides WPW syndrome and hypertrophic cardiomyopathy, PRKAG2 mutations are responsible also for a diverse phenotypes. PRKAG2 gene mutation should be suspected with familial occurrence of RBBB, sinus bradycardia, and short PR interval.

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