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Molecular Strategies for RPGR Gene Therapy
Mutations affecting the Retinitis Pigmentosa GTPase Regulator (RPGR) gene are the commonest cause of X-linked and recessive retinitis pigmentosa (RP), accounting for 10%–20% of all cases of RP. The phenotype is one of the most severe amongst all causes of RP, characteristic for its early onset and r...
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| 發表在: | Genes (Basel) |
|---|---|
| Main Authors: | , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
MDPI
2019
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6770968/ https://ncbi.nlm.nih.gov/pubmed/31487940 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes10090674 |
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