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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Phenotypic variability in three carriers from a family with choroideremia and a frameshift mutation 1388delCCinsG in

Günther Rudolph1, Markus Preising, Petros Kalpadakis

  • 1Kooperationsgruppe Ophthalmogenetik der LMU und GSF University Eye Hospital, LMU, München, Germany. Guenther.Rudolph@ak-i.med.uni-muenchen.de

Ophthalmic Genetics
|October 21, 2003
PubMed
Abstract

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