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

Παρόμοια τεκμήρια

• Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37
  ανά: Ahmed, Zubair M., κ.ά.
  Έκδοση: (2003)
• Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction
  ανά: Naz, S, κ.ά.
  Έκδοση: (2004)
• DFNB86, a novel autosomal recessive nonsyndromic deafness locus on chromosome 16p13.3
  ανά: Ali, Rana A., κ.ά.
  Έκδοση: (2011)
• Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.
  ανά: Bonné-Tamir, B., κ.ά.
  Έκδοση: (1996)
• Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23
  ανά: Bork, Julie M., κ.ά.
  Έκδοση: (2001)