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MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation.

dc.contributor.authorKalay, Ersan
dc.contributor.authorBrunner, Han
dc.contributor.authorCremers, Cor
dc.contributor.authorKaragüzel, ahmet
dc.contributor.authorKremer, Hannie
dc.contributor.authorWollnik, Bernd
dc.contributor.authorÜzümcü, Abdullah
dc.contributor.authorKrieger, E
dc.contributor.authorCaylan, R
dc.contributor.authorUlubil-Emiroğlu, Melike
dc.contributor.authorErdol, H
dc.contributor.authorBaşarer, Nermin
dc.contributor.authorHeister, Angelian
dc.contributor.authorHennies, Hans
dc.contributor.authorNürnberg, Peter
dc.contributor.authorBAŞARAN, Seher
dc.contributor.authorUYGUNER, Zehra Oya
dc.contributor.authorKAYSERİLİ, Hülya
dc.contributor.authorHafız, Günter
dc.contributor.authorHafız, Günter
dc.date.accessioned2021-03-03T15:26:54Z
dc.date.available2021-03-03T15:26:54Z
dc.identifier.citationKalay E., Üzümcü A., Krieger E., Caylan R., UYGUNER Z. O. , Ulubil-Emiroğlu M., Erdol H., Hafız G., Hafız G., Başarer N., et al., "MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation.", AMERICAN JOURNAL OF MEDICAL GENETICS, cilt.15, ss.2382-9, 2007
dc.identifier.issn0148-7299
dc.identifier.otherav_3efd4859-8721-4936-8ca5-264d564793d3
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/46174
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTemel Bilimler
dc.titleMYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation.
dc.typeMakale
dc.relation.journalAMERICAN JOURNAL OF MEDICAL GENETICS
dc.contributor.department, ,
dc.identifier.volume15
dc.identifier.startpage2382
dc.identifier.endpage9
dc.contributor.firstauthorID306428


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