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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Mucopolysaccharidosis IVA mutations in Chinese patients: 16 novel mutations

Zheng Wang1, Weimin Zhang, Yun Wang

  • 1Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, PR China.

Journal of Human Genetics
|June 25, 2010
PubMed

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