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Molecular Genetics of FAM161A in North American Patients with Early-Onset Retinitis Pigmentosa
Retinitis pigmentosa (RP) is a hereditary disease that leads to the progressive degeneration of retinal photoreceptor cells and to blindness. It is caused by mutations in several distinct genes, including the ciliary gene FAM161A, which is associated with a recessive form of this disorder. Recent in...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3961368/ https://ncbi.nlm.nih.gov/pubmed/24651477 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0092479 |
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