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Color-deficient cone mosaics associated with Xq28 opsin mutations: A stop codon versus gene deletions

Our understanding of the etiology of red-green color vision defects is evolving. While missense mutations within the long- (L-) and middle-wavelength sensitive (M-) photopigments and gross rearrangements within the L/M-opsin gene array are commonly associated with red-green defects, recent work usin...

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Detalhes bibliográficos
Main Authors: Wagner-Schuman, Melissa, Neitz, Jay, Rha, Jungtae, Williams, David R., Neitz, Maureen, Carroll, Joseph
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2975855/
https://ncbi.nlm.nih.gov/pubmed/20854834
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.visres.2010.09.015
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