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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a

Janneke M Stapelbroek1, Casper W Bollen, Johannes K Ploos van Amstel

  • 1Department of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Center, P.O. Box 85090, 3508 AB Utrecht, The Netherlands.

Journal of Hepatology
|November 3, 2004
PubMed
Abstract

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