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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Identification of novel L2HGDH gene mutations and update of the pathological spectrum

Laura Vilarinho1, Sandra Tafulo, Michelina Sibilio

  • 1Medical Genetics Center, National Health Institute-INSA, Porto, Portugal. laura.vilarinho@igm.min-saude.pt

Journal of Human Genetics
|November 14, 2009
PubMed

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