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Results 1 - 6 of 6 for Achromatopsia 4
  1. GNAT2 gene 
    The GNAT2 gene provides instructions for making one part (called the cone-specific alpha subunit) of a protein called transducin. This protein is found in ...
    https://medlineplus.gov/genetics/gene/gnat2 - Genetics
  2. OPN1SW gene 
    ... sensitive cone pigment gene associated with a tritan color vision defect. Vis Neurosci. 2006 May-Aug;23(3-4):403-9. doi: 10.1017/S0952523806233169. Citation on ...
    https://medlineplus.gov/genetics/gene/opn1sw - Genetics
  3. PDE6C gene 
    ... properties of PDE6C mutants associated with autosomal recessive achromatopsia. Hum Mol Genet. 2011 Feb 15;20(4):719-30. doi: 10.1093/hmg/ddq517. Epub ...
    https://medlineplus.gov/genetics/gene/pde6c - Genetics
  4. CNGB3 gene 
    ... Cremers FP, Klaver CC. Comprehensive analysis of the achromatopsia genes CNGA3 and CNGB3 in progressive cone dystrophy. Ophthalmology. 2010 Apr;117(4):825-30.e1. doi: 10.1016/j.ophtha. ...
    https://medlineplus.gov/genetics/gene/cngb3 - Genetics
  5. CNGA3 gene 
    ... Cremers FP, Klaver CC. Comprehensive analysis of the achromatopsia genes CNGA3 and CNGB3 in progressive cone dystrophy. Ophthalmology. 2010 Apr;117(4):825-30.e1. doi: 10.1016/j.ophtha. ...
    https://medlineplus.gov/genetics/gene/cnga3 - Genetics
  6. PDE6H gene 
    ... has been found to cause the vision disorder achromatopsia. It is a very rare cause of a form of the disorder called incomplete achromatopsia. This condition is characterized by limited color vision ...
    https://medlineplus.gov/genetics/gene/pde6h - Genetics