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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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A novel mutation in the GCM2 gene causing severe congenital isolated hypoparathyroidism

Daniel Doyle1, Susan M Kirwin, Katia Sol-Church

  • 1Division of Endocrinology, Nemours/Alfred I. duPont Hospital for Children, P.O. Box 269, Wilmington, DE 19803, USA. ddoyle@nemours.org

Journal of Pediatric Endocrinology & Metabolism : JPEM
|November 20, 2012
PubMed
Abstract

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