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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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MYO7A mutation screening in Usher syndrome type I patients from diverse origins

T Jaijo1, E Aller, M Beneyto

  • 1Unidad de Genetica, Hospital Universitario La Fe, Valencia, Spain.

Journal of Medical Genetics
|March 16, 2007
PubMed
Abstract

No abstract available in PubMed .

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