X-linked heterozygous mutations in ARR3 cause female-limited early onset high myopia

PURPOSE: To identify genetic mutations in three families with early onset high myopia (eoHM) limited to female members. METHODS: Genomic DNA was collected from participating members of families XF1, XF2, and XF3. Genome-wide linkage scans were performed on the largest family (XF1). Whole exome seque...

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Detalles Bibliográficos
Autores principales: Xiao, Xueshan, Li, Shiqiang, Jia, Xiaoyun, Guo, Xiangming, Zhang, Qingjiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082638/
https://www.ncbi.nlm.nih.gov/pubmed/27829781

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082638/
https://www.ncbi.nlm.nih.gov/pubmed/27829781

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