Associated Papers
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene.
Felden J et al.
Human Mutation, 2019
Variant phenotypes of incomplete achromatopsia in two cousins with GNAT2 gene mutations.
Rosenberg T et al.
Investigative Ophthalmology & Visual Science, 2004
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
Select a paper to view details