A Novel Mutation in the TECTA Gene in a Chinese Family with Autosomal Dominant Nonsyndromic Hearing Loss

Παρόμοια τεκμήρια

• A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family
  ανά: Bai, Haihua, κ.ά.
  Έκδοση: (2014)
• Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss
  ανά: Cui, Tian-Yi, κ.ά.
  Έκδοση: (2020)
• Targeted Gene Capture and Massively Parallel Sequencing Identify TMC1 as the Causative Gene in a Six-generation Chinese Family with Autosomal Dominant Hearing Loss
  ανά: Gao, Xue, κ.ά.
  Έκδοση: (2015)
• Novel Compound Heterozygous TMC1 Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family
  ανά: Gao, Xue, κ.ά.
  Έκδοση: (2013)
• The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss
  ανά: Yasukawa, Rika, κ.ά.
  Έκδοση: (2019)