Authors: Du Wanli, Wu Caiyun, Ma Xiaoying, Hao Shengju, Hui Ling, Fan Yujie, Zhang Qinghua
DOI: 10.3760/cma.j.cn115989-20220803-00360
Citation
Du Wanli, Wu Caiyun, Ma Xiaoying, et al. Novel SPATA7 mutations caused Leber congenital amaurosis: a case report[J]. Chin J Exp Ophthalmol, 2025, 43(10):921-923. DOI: 10.3760/cma.j.cn115989-20220803-00360.
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Authors Info & Affiliations
Du Wanli
Department of Ophthalmology, Gansu Provincial Maternity and Child-Care Hospital,Medical Genetics Center, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou 730050, China
Wu Caiyun
Department of Ophthalmology, Gansu Provincial Maternity and Child-Care Hospital,Medical Genetics Center, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou 730050, China
Ma Xiaoying
Department of Ophthalmology, Gansu Provincial Maternity and Child-Care Hospital,Medical Genetics Center, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou 730050, China
Hao Shengju
Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Lanzhou 730050, China
Hui Ling
Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Lanzhou 730050, China
Fan Yujie
Department of Ophthalmology, Gansu Provincial Maternity and Child-Care Hospital,Medical Genetics Center, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou 730050, China
Zhang Qinghua
Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Lanzhou 730050, China
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