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Comparative exome sequencing reveals novel candidate genes for retinitis pigmentosa

BACKGROUND: Retinitis pigmentosa (RP) is the most common form of inherited retinal degeneration, but genetic defects in nearly half of families remain unresolved. This study aims to identify novel genes associated with RP based on whole exome sequencing (WES) data from 552 probands with RP. METHODS:...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:EBioMedicine
Main Authors: Yi, Zhen, Ouyang, Jiamin, Sun, Wenmin, Li, Shiqiang, Xiao, Xueshan, Zhang, Qingjiong
Format: Artigo
Jezik:Inglês
Izdano: Elsevier 2020
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7248430/
https://ncbi.nlm.nih.gov/pubmed/32454406
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ebiom.2020.102792
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