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Genome-wide association study in RPGRIP1(−/−) dogs identifies a modifier locus that determines the onset of retinal degeneration
Cone-rod dystrophy (CRD) is a form of inherited retinal degeneration (RD) causing blindness in man as well as in several breeds of dog. Previously, a 44 bp insertion in RPGRIP1 (retinitis pigmentosa GTPase regulator interacting protein-1) was associated with a recessive early-onset CRD (cone-rod dys...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2011
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3947618/ https://ncbi.nlm.nih.gov/pubmed/22193413 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00335-011-9384-9 |
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