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Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.

dc.contributor.authorCremers, Cor
dc.contributor.authorUlubil-Emiroğlu, Melike
dc.contributor.authorKalay, Ersan
dc.contributor.authorLi, Y
dc.contributor.authorÜzümcü, Abdullah
dc.contributor.authorKaragüzel, ahmet
dc.contributor.authorBecker, C
dc.contributor.authorKremer, Hannie
dc.contributor.authorHafız, Günter
dc.contributor.authorKAYSERİLİ, Hülya
dc.contributor.authorUYGUNER, Zehra Oya
dc.contributor.authorBAŞARAN, Seher
dc.contributor.authorWollnik, Bernd
dc.contributor.authorCaylan, R
dc.contributor.authorNürnberg, Peter
dc.contributor.authorBaşarer, Nermin
dc.date.accessioned2021-03-02T21:22:32Z
dc.date.available2021-03-02T21:22:32Z
dc.identifier.citationKalay E., Li Y., Üzümcü A., UYGUNER Z. O. , Karagüzel a., Becker C., Cremers C., KAYSERİLİ H., Hafız G., BAŞARAN S., et al., "Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.", HUMAN MUTATION, cilt.27, ss.633-9, 2006
dc.identifier.issn1059-7794
dc.identifier.othervv_1032021
dc.identifier.otherav_06972883-3103-49ff-a01a-ef9680e285ea
dc.identifier.urihttp://hdl.handle.net/20.500.12627/10286
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.titleMutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.
dc.typeMakale
dc.relation.journalHUMAN MUTATION
dc.contributor.departmentKaradeniz Teknik Üniversitesi , ,
dc.identifier.volume27
dc.identifier.startpage633
dc.identifier.endpage9
dc.contributor.firstauthorID306434


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