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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Glycogen storage disease type II in Spanish patients: high frequency of c.1076-1G>C mutation

Laura Gort1, M Josep Coll, Amparo Chabás

  • 1Institut de Bioquímica Clínica, Hospital Clínic, C/ Mejía Lequerica s/n, Edifici Helios III, 08028 Barcelona, Spain.

Molecular Genetics and Metabolism
|July 10, 2007
PubMed

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