WNT10A missense mutation associated with a complete Odonto-Onycho-Dermal Dysplasia syndrome

Samankaltaisia teoksia

• Mutation in WNT10A Is Associated with an Autosomal Recessive Ectodermal Dysplasia: The Odonto-onycho-dermal Dysplasia
  Tekijä: Adaimy, Lynn , et al.
  Julkaistu: (2007)
• Novel missense mutation in the RSPO4 gene in congenital hyponychia and evidence for a polymorphic initiation codon (p.M1I)
  Tekijä: Khan, Tahir Naeem, et al.
  Julkaistu: (2012)
• A novel mutation in the Lipase H gene underlies autosomal recessive hypotrichosis and woolly hair
  Tekijä: Tariq, Muhammad, et al.
  Julkaistu: (2012)
• Evidence for autosomal recessive inheritance in SPG3A caused by homozygosity for a novel ATL1 missense mutation
  Tekijä: Khan, Tahir Naeem, et al.
  Julkaistu: (2014)
• Odonto-onycho-dermal dysplasia in a patient homozygous for a WNT10A nonsense mutation and mild manifestations of ectodermal dysplasia in carriers of the mutation
  Tekijä: Krøigård, Anne Bruun, et al.
  Julkaistu: (2016)