Associated Papers
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene.
Felden J et al.
Human Mutation, 2019
Genetics of color vision deficiencies.
Deeb SS et al.
Developments in Ophthalmology, 2003
Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsia.
Kohl S et al.
American Journal of Human Genetics, 2002
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