Concepedia

Publication | Closed Access

A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis

DOI

61

Citations

13

References

2006

Year

Pascal Laforêt, Pascale Richard, Mina Ait Saïd, Norma B. Romero, Emmanuelle Lacène, Jean‐Paul Leroy, Christiane Baussan, Jean‐Yves Hogrel, Thomas Lavergne, Karim Wahbi,
Neuromuscular Disorders

References

YearCitations

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