Mutational screening of AGRN, SLC39A5, SCO2, P4HA2, BSG, ZNF644, and CPSF1 in a Chinese cohort of 103 patients with nonsyndromic high myopia

PURPOSE: High myopia (HM) is one of the leading causes of irreversible vision loss in the world. Many myopia loci have been uncovered with linkage analysis, genome-wide association studies, and sequencing analysis. Numerous pathogenic genes within these loci have been detected in a portion of HM cas...

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Detalles Bibliográficos
Autores principales: Zheng, Yi-Han, Cai, Xue-Bi, Xia, Lu-Qi, Zhou, Fang-Yue, Wen, Xin-Ran, Chen, De-Fu, Han, Fang, Zhou, Kai-Jing, Jin, Zi-Bing, Zhuang, Wen-Juan, Lin, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8684808/
https://www.ncbi.nlm.nih.gov/pubmed/35002215

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