Pathogenic mutations in TULP1 responsible for retinitis pigmentosa identified in consanguineous familial cases

Παρόμοια τεκμήρια

• Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases
  ανά: Kabir, Firoz, κ.ά.
  Έκδοση: (2016)
• Mutations in phosphodiesterase 6 identified in familial cases of retinitis pigmentosa
  ανά: Ullah, Inayat, κ.ά.
  Έκδοση: (2016)
• Association of Pathogenic Mutations in TULP1 With Retinitis Pigmentosa in Consanguineous Pakistani Families
  ανά: Iqbal, Muhammad, κ.ά.
  Έκδοση: (2011)
• Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindness
  ανά: Naeem, Muhammad Asif, κ.ά.
  Έκδοση: (2015)
• Mutations in CERKL and RP1 cause retinitis pigmentosa in Pakistani families
  ανά: Nadeem, Raheela, κ.ά.
  Έκδοση: (2020)