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Updated: Feb 17, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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A novel mutation of HOXA11 in a patient with septate uterus

Ying Zhu1, Zhi Cheng2,3, Jing Wang3

  • 1Reproductive Medicine Center, The First Affiliated Hospital, Anhui Medical University, Hefei, 230032, People's Republic of China.

Orphanet Journal of Rare Diseases
|December 13, 2017
PubMed
Abstract

Keywords:
HOXA11MutationSeptate uterus patients

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