SNRNP200 Mutations Cause Autosomal Dominant Retinitis Pigmentosa

SNRNP200 Mutations Cause Autosomal Dominant Retinitis Pigmentosa

The small nuclear ribonucleoprotein 200 kDa (SNRNP200) gene plays a key role in the maturation of pre-message RNA (pre-mRNA) splicing with the indication for the etiology of retinitis pigmentosa (RP). Gene recognition can facilitate the diagnosis of these patients for better clinical management, tre...

Full description

Bibliographic Details
Main Authors: Tao Zhang, Jingshan Bai, Xinyi Zhang, Xiaowei Zheng, Nan Lu, Zhongyin Liang, Ling Lin, Yongsong Chen
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-01-01
Series:Frontiers in Medicine
Subjects:
retinitis pigmentosa
SNRNP200
whole exome sequencing
mutation
morpholino oligonucleotide
Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2020.588991/full

Similar Items

Similar Items