Publication:
Jeune Syndrome with a novel DYNC2H1 mutation

Simple item page
dc.contributor.authorsElcioglu, N. H.; Yeter, B.; Xue, J. Y.; Wang, Z.; Guo, L.; Nishimura, G.; Ikegawa, S.
dc.date.accessioned2022-03-10T18:00:47Z
dc.date.accessioned2026-01-11T19:01:20Z
dc.date.available2022-03-10T18:00:47Z
dc.date.issued2020
dc.identifier.doidoiWOS:000598482603078
dc.identifier.eissn1476-5438
dc.identifier.issn1018-4813
dc.identifier.urihttps://hdl.handle.net/11424/222316
dc.identifier.wosWOS:000598482603078
dc.language.isoeng
dc.publisherSPRINGERNATURE
dc.relation.ispartofEUROPEAN JOURNAL OF HUMAN GENETICS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleJeune Syndrome with a novel DYNC2H1 mutation
dc.typeconferenceObject
dc.type.submeetingabstract
dspace.entity.typePublication
oaire.citation.endPage836
oaire.citation.issueSUPPL 1
oaire.citation.startPage835
oaire.citation.titleEUROPEAN JOURNAL OF HUMAN GENETICS
oaire.citation.volume28

Files

Collections

Araştırma Çıktıları