Recurrent and Private MY015A Mutations Are Associated with Deafness in the Turkish Population
Recurrent and Private MY015A Mutations Are Associated with Deafness in the Turkish Population
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Author / Creator
Cengiz, F B , Duman, D , Sirmaci, A , Tokgoez-Yilmaz, S , Erbek, S , Oeztuerkmen-Akay, H , Incesulu, A , Edwards, YJK , Oezda, H , Liu, X Z and Tekin, M
Journal title
Language
English
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Scope and Contents
Contents
The identities and frequencies of MYO15A mutations associated with hearing loss in different populations remained largely unknown. We screened the MYO15A gene for mutations in 104 unrelated multiplex and consanguineous Turkish families with autosomal recessive nonsyndromic sensorineural hearing loss using autozygosity mapping. The screening of MYO1...
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Full title
Recurrent and Private MY015A Mutations Are Associated with Deafness in the Turkish Population
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Record Identifier
TN_cdi_proquest_miscellaneous_954638048
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_954638048
Other Identifiers
ISSN
1945-0265
DOI
10.1089/gtmb.2010.0039
