Nonsense mutation in MERTK causes autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family

Documenti analoghi

• Mutations in the β-subunit of rod phosphodiesterase identified in consanguineous Pakistani families with autosomal recessive retinitis pigmentosa
  di: Ali, Shahbaz, et al.
  Pubblicazione: (2011)
• Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family
  di: Kaul, Haiba, et al.
  Pubblicazione: (2010)
• Association of Pathogenic Mutations in TULP1 With Retinitis Pigmentosa in Consanguineous Pakistani Families
  di: Iqbal, Muhammad, et al.
  Pubblicazione: (2011)
• Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1
  di: Yasmeen, Afshan, et al.
  Pubblicazione: (2010)
• A Novel Locus for Autosomal Recessive Retinitis Pigmentosa in a Consanguineous Pakistani Family Maps to Chromosome 2p
  di: NAZ, SHAGUFTA, et al.
  Pubblicazione: (2010)