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Further evidence of involvement of CDC14A in autosomal recessive non-syndromic hearing loss

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dc.contributor.authorDoll, J.-
dc.contributor.authorKolb, S.-
dc.contributor.authorSchnapp, L.-
dc.contributor.authorRad, A.-
dc.contributor.authorRueschendorf, F.-
dc.contributor.authorKhan, I.-
dc.contributor.authorAdli, A.-
dc.contributor.authorHasanzadeh, A.-
dc.contributor.authorLiedtke, D.-
dc.contributor.authorKnaup, S.-
dc.contributor.authorHofrichter, M. A. H.-
dc.contributor.authorMueller, T.-
dc.contributor.authorDittrich, M.-
dc.contributor.authorKong, I.-
dc.contributor.authorKim, H.-
dc.contributor.authorHaaf, T.-
dc.contributor.authorVona, B.-
dc.date.accessioned2022-12-26T12:15:52Z-
dc.date.available2022-12-26T12:15:52Z-
dc.date.issued2020-12-
dc.identifier.issn1018-4813-
dc.identifier.issn1476-5438-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/5886-
dc.format.extent1-
dc.language영어-
dc.language.isoENG-
dc.publisherNatue Publishing Group-
dc.titleFurther evidence of involvement of CDC14A in autosomal recessive non-syndromic hearing loss-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.wosid000598482600346-
dc.identifier.bibliographicCitationEuropean Journal of Human Genetics, v.28, no.SUPPL 1, pp 188 - 188-
dc.citation.titleEuropean Journal of Human Genetics-
dc.citation.volume28-
dc.citation.numberSUPPL 1-
dc.citation.startPage188-
dc.citation.endPage188-
dc.type.docTypeMeeting Abstract-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaGenetics & Heredity-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryGenetics & Heredity-
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