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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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Dettagli Bibliografici
Pubblicato in:Mol Vis
Autori principali: Xiao, Xueshan, Li, Shiqiang, Jia, Xiaoyun, Guo, Xiangming, Zhang, Qingjiong
Natura: Artigo
Lingua:Inglês
Pubblicazione: Molecular Vision 2016
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5082638/
https://ncbi.nlm.nih.gov/pubmed/27829781
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