Mutations in GJB2, TMC1, TMPRSS3 and MYO15A cause autosomal recessive nonsyndromic hearing loss in Turkish patients.


KALAY E.

European Human Genetics Conference, Amsterdam, Netherlands, 6 - 09 May 2006, pp.141

  • Publication Type: Conference Paper / Full Text
  • City: Amsterdam
  • Country: Netherlands
  • Page Numbers: pp.141