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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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A case of congenital glycogen storage disease type IV with a novel GBE1 mutation

G Praveen Raju1, Hsin-Chang Li, Deeksha S Bali

  • 1Department of Neurology, Children's Hospital Boston and Harvard Medical School, 300 Longwood Avenue, Boston, MA, USA.

Journal of Child Neurology
|January 31, 2008
PubMed

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