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Identification of a novel NRL mutation in a Chinese family with retinitis pigmentosa by whole-exome sequencing.

ABSTRACT:

SUBMITTER: Qin Y 

PROVIDER: S-EPMC5437331 | biostudies-literature | 2017 May

REPOSITORIES: biostudies-literature

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Identification of a novel NRL mutation in a Chinese family with retinitis pigmentosa by whole-exome sequencing.

Qin Y Y   Liu F F   Yu S S   Yang L L   Gao M M   Tang Z Z   Guo A Y AY   Zhang M M   Li P P   Liu M M  

Eye (London, England) 20170120 5

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