Other names: Achromatopsia-3,
Affected gene: CNGB3
Inheritance: Autosomal recessive
Mutation: CanFam3.1 29 g.32837065C>T c.784G>A
OMIA link: 001365-9615

Breeds suitable for testing : German Shorthaired Pointer

Reference:
Sidjanin, D.J., Lowe, J.K., McElwee, J.L., Milne, B.S., Phippen, T.M., Sargan, D.R., Aguirre, G.D., Acland, G.M., Ostrander, E.A. :    
Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3 Human Molecular Genetics 11:1823-33, 2002. Pubmed reference: 12140185.