Novel CNGA3 and CNGB3 mutations in two Pakistani families with achromatopsia

Samankaltaisia teoksia

• Achromatopsia caused by novel mutations in both CNGA3 and CNGB3
  Tekijä: Johnson, S, et al.
  Julkaistu: (2004)
• A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family
  Tekijä: Azam, Maleeha, et al.
  Julkaistu: (2009)
• Intraobserver Repeatability and Interobserver Reproducibility of Foveal Cone Density Measurements in CNGA3- and CNGB3-Associated Achromatopsia
  Tekijä: Georgiou, Michalis, et al.
  Julkaistu: (2020)
• Erratum in: Intraobserver Repeatability and Interobserver Reproducibility of Foveal Cone Density Measurements in CNGA3- and CNGB3-Associated Achromatopsia
  Julkaistu: (2020)
• A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa
  Tekijä: Azam, Maleeha, et al.
  Julkaistu: (2009)