A novel mutation in 3’UTR of GJB2 gene in autosomal recessive nonsyndromic sensorineural hearing loss in South Indian population

Lignende værker

• Evaluation of the GJB2 and GJB6 Polymorphisms with Autosomal Recessive Nonsyndromic Hearing Loss in Iranian Population
  af: Ebrahimkhani, Somayeh, et al.
  Udgivet: (2021)
• MITF variants cause nonsyndromic sensorineural hearing loss with autosomal recessive inheritance
  af: Thongpradit, Supranee, et al.
  Udgivet: (2020)
• Single Nucleotide Polymorphisms of the GJB2 and GJB6 Genes Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss
  af: Grillo, Ana Paula, et al.
  Udgivet: (2015)
• A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss
  af: Sırmacı, Aslı, et al.
  Udgivet: (2010)
• Histopathology of Nonsyndromic Autosomal Dominant Midfrequency Sensorineural Hearing Loss
  af: Bahmad, Fayez, et al.
  Udgivet: (2008)