Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness

نویسندگان

  • Zied Riahi
  • Crystel Bonnet
  • Rim Zainine
  • Malek Louha
  • Yosra Bouyacoub
  • Nadia Laroussi
  • Mariem Chargui
  • Rym Kefi
  • Laurence Jonard
  • Imen Dorboz
  • Jean-Pierre Hardelin
  • Sihem Belhaj Salah
  • Jacqueline Levilliers
  • Dominique Weil
  • Kenneth McElreavey
  • Odile Tanguy Boespflug
  • Ghazi Besbes
  • Sonia Abdelhak
  • Christine Petit
چکیده

Identification of the causative mutations in patients affected by autosomal recessive non syndromic deafness (DFNB forms), is demanding due to genetic heterogeneity. After the exclusion of GJB2 mutations and other mutations previously reported in Tunisian deaf patients, we performed whole exome sequencing in patients affected with severe to profound deafness, from four unrelated consanguineous Tunisian families. Four biallelic non previously reported mutations were identified in three different genes: a nonsense mutation, c.208C>T (p.R70X), in LRTOMT, a missense mutation, c.5417T>C (p.L1806P), in MYO15A and two splice site mutations, c.7395+3G>A, and c.2260+2T>A, in MYO15A and TMC1 respectively. We thereby provide evidence that whole exome sequencing is a powerful, cost-effective screening tool to identify mutations causing recessive deafness in consanguineous families.

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عنوان ژورنال:

دوره 9  شماره 

صفحات  -

تاریخ انتشار 2014