Lack of significant association between mutations of KCNJ10 or FOXI1 and SLC26A4 mutations in pendred syndrome/enlarged vestibular aqueducts

Lignende værker

• Genetic heterogeneity in patients with enlarged vestibular aqueduct and Pendred syndrome
  af: Marek Sklenar, et al.
  Udgivet: (2025-05-01)
• Transcriptional Control of SLC26A4 Is Involved in Pendred Syndrome and Nonsyndromic Enlargement of Vestibular Aqueduct (DFNB4)
  af: Yang, Tao , et al.
  Udgivet: (2007)
• Mutations of KCNJ10 Together with Mutations of SLC26A4 Cause Digenic Nonsyndromic Hearing Loss Associated with Enlarged Vestibular Aqueduct Syndrome
  af: Yang, Tao, et al.
  Udgivet: (2009)
• Mutation analysis of SLC26A4 in patients with enlarged vestibular aqueduct in mainland China
  af: Reyes, Samuel, et al.
  Udgivet: (2009)
• SLC26A4 mutation testing for hearing loss associated with enlargement of the vestibular aqueduct
  af: Ito, Taku, et al.
  Udgivet: (2013)