Clinical and genetic analysis VSX1 variants among families with keratoconus in northwest China

Purpose: To screen VSX1 gene sequence variations and describe the clinical features of families with keratoconus (KC) from northwest China. Methods: We screened VSX1 sequence variations and clinical data of 37 families including 37 probands with diagnosed KC from Ningxia Eye Hospital (China). VSX1 w...

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Detalles Bibliográficos
Autores principales: Zhang, Jinjin, Cai, Bo, Ma, Limei, Qin, Yixuan, Li, Shuai, Sun, Caihong, Liang, Jing, Han, Yu, Zhuang, Wenjuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043922/
https://www.ncbi.nlm.nih.gov/pubmed/36999054
http://dx.doi.org/10.3389/fgene.2023.1145426

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043922/
https://www.ncbi.nlm.nih.gov/pubmed/36999054
http://dx.doi.org/10.3389/fgene.2023.1145426

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