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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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| Published in: | Front Med (Lausanne) |
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| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
Frontiers Media S.A.
2021
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7859630/ https://ncbi.nlm.nih.gov/pubmed/33553197 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fmed.2020.588991 |
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