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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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CHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophy
Godelieve Morel1, Cécile Rouzier1,2, Annabelle Chaussenot1,2
1Department of Medical Genetics, National Center for Mitochondrial Diseases, Nice Teaching Hospital, Nice, France.
Annals of Neurology
|June 23, 2015
Abstract
No abstract available in PubMed .
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