Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly

Lignende værker

• Mutations in <it>WDR62 </it>gene in Pakistani families with autosomal recessive primary microcephaly
  af: Mir Asif, et al.
  Udgivet: (2011-10-01)
• Autosomal recessive primary microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum
  af: Mahmood, Saqib, et al.
  Udgivet: (2011)
• A Recurrent Intragenic Deletion Mutation in DSG4 Gene in Three Pakistani Families with Autosomal Recessive Hypotrichosis
  af: Rafiq, Muhammad Arshad, et al.
  Udgivet: (2004)
• Previously described sequence variant in CDK5RAP2 gene in a Pakistani family with autosomal recessive primary microcephaly
  af: Hassan, Muhammad Jawad, et al.
  Udgivet: (2007)
• WDR62 is associated with the spindle pole and is mutated in human microcephaly
  af: Nicholas, Adeline K, et al.
  Udgivet: (2010)