Cone photoreceptor mosaic disruption associated with Cys203Arg mutation in the M-cone opsin

Missense mutations in the cone opsins have been identified as a relatively common cause of red/green color vision defects, with the most frequent mutation being the substitution of arginine for cysteine at position 203 (C203R). When the corresponding cysteine is mutated in rhodopsin, it disrupts pro...

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Detalhes bibliográficos
Main Authors: Carroll, Joseph, Baraas, Rigmor C., Wagner-Schuman, Melissa, Rha, Jungtae, Siebe, Cory A., Sloan, Christina, Tait, Diane M., Thompson, Summer, Morgan, Jessica I. W., Neitz, Jay, Williams, David R., Foster, David H., Neitz, Maureen
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2009
Assuntos:
Biological Sciences
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2791574/
https://ncbi.nlm.nih.gov/pubmed/19934058
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0910128106
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