Mutations in C2ORF71 Cause Autosomal-Recessive Retinitis Pigmentosa

Παρόμοια τεκμήρια

• Identification of a novel nonsense mutation in RP1 that causes autosomal recessive retinitis pigmentosa in an Indonesian family
  ανά: Siemiatkowska, Anna M., κ.ά.
  Έκδοση: (2012)
• Missense mutations at homologous positions in the fourth and fifth laminin A G-like domains of eyes shut homolog cause autosomal recessive retinitis pigmentosa
  ανά: Khan, Muhammad Imran, κ.ά.
  Έκδοση: (2010)
• Identification of a 2 Mb Human Ortholog of Drosophila eyes shut/spacemaker that Is Mutated in Patients with Retinitis Pigmentosa
  ανά: Collin, Rob W.J., κ.ά.
  Έκδοση: (2008)
• Autosomal-Recessive Early-Onset Retinitis Pigmentosa Caused by a Mutation in PDE6G, the Gene Encoding the Gamma Subunit of Rod cGMP Phosphodiesterase
  ανά: Dvir, Liron, κ.ά.
  Έκδοση: (2010)
• Lighting a candle in the dark: advances in genetics and gene therapy of recessive retinal dystrophies
  ανά: den Hollander, Anneke I., κ.ά.
  Έκδοση: (2010)