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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Myosin storage myopathy: slow skeletal myosin (MYH7) mutation in two isolated cases

N G Laing1, C Ceuterick-de Groote, D E Dye

  • 1Centre for Neuromuscular and Neurologic Disorders, Australian Neuromuscular Research Institute and Centre for Medical Research, University of Western Australia, QEII Medical Centre, Nedlands, Australia. nlaing@cyllene.uwa.edu.au

Neurology
|February 9, 2005
PubMed

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