Transcriptional Control of SLC26A4 Is Involved in Pendred Syndrome and Nonsyndromic Enlargement of Vestibular Aqueduct (DFNB4)

This publication has 27 references indexed in Scilit:

• Epididymal expression of the forkhead transcription factor Foxi1 is required for male fertility
  The EMBO Journal, 2006
• Expression of GJB2 and GJB6 Is Reduced in a Novel DFNB1 Allele
  American Journal of Human Genetics, 2006
• Structure of the Forkhead Domain of FOXP2 Bound to DNA
  Structure, 2006
• The forkhead transcription factor Foxi1 directly activates the AE4 promoter
  Biochemical Journal, 2005
• Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity
  Clinical Genetics, 2004
• Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese
  European Journal of Human Genetics, 2003
• Pendred syndrome and DFNB4‐mutation screening of SLC26A4 by denaturing high‐performance liquid chromatography and the identification of eleven novel mutations
  American Journal of Medical Genetics Part A, 2003
• Pendred syndrome, DFNB4, andPDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations
  Human Mutation, 2001
• A mutation in PDS causes non-syndromic recessive deafness
  Nature Genetics, 1998
• Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)
  Nature Genetics, 1997