Mutations in GJB2, TMC1, TMPRSS3 and MYO15A cause autosomal recessive nonsyndromic hearing loss in Turkish patients.
Copy For Citation
KALAY E.
European Human Genetics Conference, Amsterdam, Netherlands, 6 - 09 May 2006, pp.141
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Publication Type:
Conference Paper / Full Text
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City:
Amsterdam
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Country:
Netherlands
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Page Numbers:
pp.141
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Karadeniz Technical University Affiliated:
Yes