A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene-Reference-Cited by-同舟云学术

A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene

Published:2009-11-03 Issue:46 Volume:106 Page:19581-19586
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Chang B.,Grau T.,Dangel S.,Hurd R.,Jurklies B.,Sener E. C.,Andreasson S.,Dollfus H.,Baumann B.,Bolz S.,Artemyev N.,Kohl S.,Heckenlively J.,Wissinger B.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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4. CNGB3Achromatopsia with Progressive Loss of Residual Cone Function and Impaired Rod-Mediated Function

5. Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel

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