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Genes and mutations causing retinitis pigmentosa

Retinitis pigmentosa (RP) is a heterogeneous set of inherited retinopathies with many disease-causing genes, many known mutations, and highly varied clinical consequences. Progress in finding treatments is dependent on determining the genes and mutations causing these diseases, which includes both g...

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Detalhes bibliográficos
Main Authors: Daiger, SP, Sullivan, LS, Bowne, SJ
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3856531/
https://ncbi.nlm.nih.gov/pubmed/23701314
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cge.12203
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