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

✍ Scribed by Pascal Laforêt; Pascale Richard; Mina Ait Said; Norma Beatriz Romero; Emmanuelle Lacene; Jean-Paul Leroy; Christiane Baussan; Jean-Yves Hogrel; Thomas Lavergne; Karim Wahbi; Bernard Hainque; Denis Duboc

Book ID: 116792406
Publisher: Elsevier Science
Year: 2006
Tongue: English
Weight: 221 KB
Volume: 16
Category: Article
ISSN: 0960-8966
DOI: 10.1016/j.nmd.2005.12.004

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