Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

Liknande verk

• Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts
  av: Irum, Bushra, et al.
  Publicerad: (2016)
• Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts
  av: Irum, Bushra, et al.
  Publicerad: (2016)
• A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
  av: Rauf, Bushra, et al.
  Publicerad: (2016)
• Novel mutations in LTBP2 identified in familial cases of primary congenital glaucoma
  av: Rauf, Bushra, et al.
  Publicerad: (2020)
• Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophy
  av: Kabir, Firoz, et al.
  Publicerad: (2013)