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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with

Borut Peterlin1, Mojca Globočnik Petrovič2, Jana Makuc1

  • 1Division of Medical Genetics, Department of Obstetrics and Gynecology, University Medical Centre, Ljubljana, Slovenia.

Journal of Human Genetics
|November 18, 2003
PubMed

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