Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction

Podobne zapisy

• Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness
  od: Ben-Yosef, T., i wsp.
  Wydane: (2001)
• Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37
  od: Ahmed, Zubair M., i wsp.
  Wydane: (2003)
• Mutations in PTPRQ Are a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB84 and Associated with Vestibular Dysfunction
  od: Schraders, Margit, i wsp.
  Wydane: (2010)
• Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts
  od: Chen, Jianjun, i wsp.
  Wydane: (2011)
• Mutation of ATF6 causes autosomal recessive achromatopsia
  od: Ansar, Muhammad, i wsp.
  Wydane: (2015)