Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness

Gelijkaardige items

• Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37
  door: Ahmed, Zubair M., et al.
  Gepubliceerd in: (2003)
• Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction
  door: Naz, S, et al.
  Gepubliceerd in: (2004)
• Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.
  door: Bonné-Tamir, B., et al.
  Gepubliceerd in: (1996)
• DFNB86, a novel autosomal recessive nonsyndromic deafness locus on chromosome 16p13.3
  door: Ali, Rana A., et al.
  Gepubliceerd in: (2011)
• Vestibular Dysfunction in DFNB1 deafness
  door: Dodson, Kelley M, et al.
  Gepubliceerd in: (2011)