Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Zhuo-Kun Feng"'
Autor:
Ke Xu, De-Fu Chen, Haoyu Chang, Ren-Juan Shen, Hua Gao, Xiao-Fang Wang, Zhuo-Kun Feng, Xiaohui Zhang, Yue Xie, Yang Li, Zi-Bing Jin
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
PurposeThe aim of this study was to probe the global profile of the EYS-associated genotype-phenotype trait in the worldwide reported IRD cases and to build a model for predicting disease progression as a reference for clinical consultation.MethodsTh
Externí odkaz:
https://doaj.org/article/757717f6b6124396a2a7a221922c73f5
Autor:
Xiao-Fang Wang, Hui Chen, Peng-Juan Huang, Zhuo-Kun Feng, Zi-Qi Hua, Xiang Feng, Fang Han, Xiao-Tao Xu, Ren-Juan Shen, Yang Li, Zi-Bing Jin, Huan-Yun Yu
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Purpose: Congenital nystagmus (CN) is a genetically and clinically heterogeneous ocular disorder that manifests as involuntary, periodic oscillations of the eyes. To date, only FRMD7 and GPR143 have been reported to be responsible for causing CN. Her
Externí odkaz:
https://doaj.org/article/1a823d01953d4612a7c61a9c11a506b6
Autor:
Keng-Hung Lin, Ren‐Juan Shen, Zhi-Qin Huang, Shi-Huang Lee, Zhuo-Kun Feng, Xiu-Feng Huang, Xiao-Fang Wang, Zi-Bing Jin, Zhen-Ji Chen
Publikováno v:
Clinical & Experimental Ophthalmology. 48:486-499
Background Inherited retinal dystrophy (IRD) is a group of irreversible retinal degenerative disorders with significant genotypic and phenotypic heterogeneity, which cause difficulty in making a precise clinical diagnosis. Furthermore, the mutation s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae4590b44295672d2e6b6fe4c63ef05b
https://doi.org/10.1111/ceo.13708
https://doi.org/10.1111/ceo.13708
Autor:
Zhuo-Kun Feng, Xiaohui Zhang, Yang Li, Hua Gao, Yue Xie, De-Fu Chen, Ren-Juan Shen, Haoyu Chang, Zi-Bing Jin, Ke Xu, Xiao-Fang Wang
Publikováno v:
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
PurposeThe aim of this study was to probe the global profile of the EYS-associated genotype-phenotype trait in the worldwide reported IRD cases and to build a model for predicting disease progression as a reference for clinical consultation.MethodsTh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ed389818afcc7af3152b69a955cd27f
https://doi.org/10.3389/fcell.2021.634220
https://doi.org/10.3389/fcell.2021.634220