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...

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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

Internet

https://www.frontiersin.org/articles/10.3389/fmed.2020.588991/full

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