Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families

Lignende værker

• A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
  af: Micheal, Shazia, et al.
  Udgivet: (2016)
• Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
  af: Micheal, Shazia, et al.
  Udgivet: (2016)
• Effects of Artisan aphakic intraocular lens on central corneal thickness and intra ocular pressure in pediatric eyes with crystalline subluxated lenses
  af: Zafar, Saemah Nuzhat, et al.
  Udgivet: (2013)
• Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld–Rieger syndrome
  af: Micheal, Shazia, et al.
  Udgivet: (2015)
• Novel variants underlying autosomal recessive intellectual disability in Pakistani consanguineous families
  af: Ilyas, Muhammad, et al.
  Udgivet: (2020)