Učitavanje...
Molecular studies of phenotype variation in canine RPGR-XLPRA1
PURPOSE: Canine X-linked progressive retinal atrophy 1 (XLPRA1) caused by a mutation in retinitis pigmentosa (RP) GTPase regulator (RPGR) exon ORF15 showed significant variability in disease onset in a colony of dogs that all inherited the same mutant X chromosome. Defective protein trafficking has...
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| Izdano u: | Mol Vis |
|---|---|
| Glavni autori: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Molecular Vision
2016
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4830396/ https://ncbi.nlm.nih.gov/pubmed/27122963 |
| Oznake: |
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