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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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CYP17A1 mutations identified in 17 Chinese patients with 17α-hydroxylase/17,20-lyase deficiency

Fengxia Yao1, Shangzhi Huang, Xiaodi Kang

  • 1Clinical Research Lab, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.

Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|September 8, 2012
PubMed
Abstract

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