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Adaptive optics retinal imaging reveals S-cone dystrophy in tritan color-vision deficiency

Tritan color-vision deficiency is an autosomal dominant disorder associated with mutations in the short-wavelength-sensitive- (S-) cone-pigment gene. An unexplained feature of the disorder is that individuals with the same mutation manifest different degrees of deficiency. To date, it has not been p...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Baraas, Rigmor C., Carroll, Joseph, Gunther, Karen L., Chung, Mina, Williams, David R., Foster, David H., Neitz, Maureen
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2007
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2082754/
https://ncbi.nlm.nih.gov/pubmed/17429491
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