PITX3 mutations associated with autosomal dominant congenital cataract in the Chinese population-Reference-Cited by-同舟云学术

PITX3 mutations associated with autosomal dominant congenital cataract in the Chinese population

Published:2019-02-26 Issue: Volume: Page:
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:
Short-container-title:Mol Med Report

Author:

Wu Zehua¹,Meng Delong¹,Fang Chengbo²,Li Jian³,Zheng Xiujie¹,Lin Jiansuo¹,Zeng Haijiang⁴,Lv Sihan³,Zhang Zhenning⁵,Luan Bing³,Zhong Zilin¹,Chen Jianjun¹

Affiliation:

1. Department of Ophthalmology, Shanghai Tenth People's Hospital and Tongji Eye Institute, Tongji University School of Medicine, Shanghai 200092, P.R. China

2. Department of Ophthalmology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230032, P.R. China

3. Department of Endocrinology, Shanghai Tenth People's Hospital and Tongji Eye Institute, Tongji University School of Medicine, Shanghai 200092, P.R. China

4. Department of Pediatrics, Ganzhou People's Hospital, Ganzhou, Jiangxi 341000, P.R. China

5. Translational Medical Center for Stem Cell Therapy and Institute for Regenerative Medicine, Shanghai East Hospital, Shanghai Key Laboratory of Signaling and Disease Research, School of Life Science and Technology, Tongji University, Shanghai 200092, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

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