https://pubmed.ncbi.nlm.nih.gov/17265047/
Achromatopsia: the CNGB3 p.T383fsX mutation results from a founder effect and is responsible for...
Achromatopsia (ACHM) or rod monochromacy is an autosomal recessive and genetically heterogeneous retinal disorder. It is characterized by a lack of color...
https://scholarshare.temple.edu/items/8faca7c0-8b16-4d12-8fcd-bfde5f79d94d
EXPRESSION OF THE CNGB3 SUBUNIT IN RETINA OF ACHROMATOPSIA-AFFECTED DOGS
Light energy is converted into an electrical signal by a set of proteins in the phototransduction cascade in photoreceptors. In this work, I focus on two...
of theexpressionsubunitretinaachromatopsia
https://tobias-lib.uni-tuebingen.de/xmlui/handle/10900/129838
A deep intronic substitution in CNGB3 is one of the major causes of achromatopsia among Jewish...