A new locus for autosomal recessive congenital cataract identified in a Pakistani family

Liknande verk

• Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1
  av: Yasmeen, Afshan, et al.
  Publicerad: (2010)
• Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family
  av: Kaul, Haiba, et al.
  Publicerad: (2010)
• Mutations in the β-subunit of rod phosphodiesterase identified in consanguineous Pakistani families with autosomal recessive retinitis pigmentosa
  av: Ali, Shahbaz, et al.
  Publicerad: (2011)
• Nonsense mutation in MERTK causes autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family
  av: Shahzadi, Amber, et al.
  Publicerad: (2010)
• Ectopia Lentis in a Consanguineous Pakistani Family and a Novel Locus on Chromosome 8q
  av: Kaul, Haiba, et al.
  Publicerad: (2010)