A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family

Παρόμοια τεκμήρια

• Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian population
  ανά: Hildebrand, Michael S., κ.ά.
  Έκδοση: (2010)
• Mutations in the MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss
  ανά: Shearer, A. Eliot, κ.ά.
  Έκδοση: (2009)
• Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation
  ανά: Hildebrand, Michael S., κ.ά.
  Έκδοση: (2010)
• Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42
  ανά: Borck, Guntram, κ.ά.
  Έκδοση: (2011)
• A Novel Mutation in COCH – Implications for Genotype-Phenotype Correlations in DFNA9 Hearing Loss
  ανά: Hildebrand, Michael S., κ.ά.
  Έκδοση: (2010)