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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Familial cylindromatosis

C Stoll1, Y Alembik, A Wilk

  • 1Service de Génétique Médicale, Strasbourg Hôpital de Hautepierre. Claude.Stoll@chru-strasbourg.fr

Genetic Counseling (Geneva, Switzerland)
|August 4, 2004
PubMed

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