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Identification of a new mutant allele, Grm6(nob7), for complete congenital stationary night blindness

Electroretinogram (ERG) studies identified a new mouse line with a normal a-wave but lacking the b-wave component. The ERG phenotype of this new allele, nob7, matched closely that of mouse mutants for Grm6, Lrit3, Trpm1, and Nyx, which encode for proteins expressed in depolarizing bipolar cells (DBC...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Vis Neurosci
Egile Nagusiak: QIAN, HAOHUA, JI, RUI, GREGG, RONALD G., PEACHEY, NEAL S.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2015
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4648616/
https://ncbi.nlm.nih.gov/pubmed/26241901
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S0952523815000012
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