Homozygotes for a R869G Mutation in the β -myosin Heavy Chain Gene have a Severe Form of Familial Hypertrophic Cardiomyopathy

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Homozygotes for a R869G Mutation in the β -myosin Heavy Chain Gene have a Severe Form of Familial Hypertrophic Cardiomyopathy is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1006/JMCC.2000.1193
P698PubMed publication ID10900182

P50authorPhilippe CharronQ51581875
Michel KomajdaQ64498753
Bernard HainqueQ114341544
Céline LedeuilQ114385008
Jean-Brieuc BouhourQ114385015
P2093author name stringOlivier Dubourg
Lucie Carrier
Michel Desnos
Ketty Schwartz
Christophe Leclercq
Pascale Richard
Jean Claude Daubert
P433issue8
P921main subjectfamilial hypertrophic cardiomyopathyQ56014654
hypertrophic cardiomyopathyQ1364270
P304page(s)1575-1583
P577publication date2000-08-01
P1433published inJournal of Molecular and Cellular CardiologyQ2061932
P1476titleHomozygotes for a R869G Mutation in the β -myosin Heavy Chain Gene have a Severe Form of Familial Hypertrophic Cardiomyopathy
P478volume32

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cites work (P2860)
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Q59461126Genomic medicine and atrial fibrillation**Editorials published in the Journal of the American College of Cardiologyreflect the views of the authors and do not necessarily represent the views of JACCor the American College of Cardiology
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