Comment on homozygosity mapping of a consanguineous Pakistani family affected with oculocutaneous albinism to Tyrosinase gene

Lignende værker

• Homozygosity mapping of a consanguineous Pakistani family affected with oculocutaneous albinism to Tyrosinase gene
  af: Shakil, Muhammad, et al.
  Udgivet: (2016)
• Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA).
  af: Tripathi, R K, et al.
  Udgivet: (1993)
• Homozygosity mapping identified a novel protein truncating mutation (p.Ser100Leufs*24) of the BBS9 gene in a consanguineous Pakistani family with Bardet Biedl syndrome
  af: Khan, Muzammil Ahmad, et al.
  Udgivet: (2016)
• Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families
  af: Li, Lin, et al.
  Udgivet: (2017)
• Genetic Causes of Oculocutaneous Albinism in Pakistani Population
  af: Sajid, Zureesha, et al.
  Udgivet: (2021)