Prp8 Retinitis Pigmentosa Mutants Cause Defects in the Transition between the Catalytic Steps of Splicing

Name: Prp8 Retinitis Pigmentosa Mutants Cause Defects in the Transition between the Catalytic Steps of Splicing
Published: 2016-07-21T00:00:00+08:00

ChEBI2016-07-21 更新2026-07-12 收录

遗传性视网膜疾病

RNA剪接

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-75081 数据链接链接失效反馈

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资源简介：

Prp8 Retinitis Pigmentosa Mutants Cause Defects in the Transition between the Catalytic Steps of Splicing

创建时间：

2016-07-21

Prp8 Retinitis Pigmentosa Mutants Cause Defects in the Transition between the Catalytic Steps of Splicing

资源简介：

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