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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type I

A Oshima1, T Jaijo, E Aller

  • 1Center for the Study and Treatment of Usher Syndrome, Boys Town National research hospital, Omaha, Nebraska 68131, USA.

Human Mutation
|April 23, 2008
PubMed

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