A novel mutation in the coiled-coil interaction domain of LAMB1 extends the molecular basis of laminin-related cortical malformation phenotypes

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dc.authorwosidYılmaz, Elmasnur/ABH-3317-2020
dc.authorwosidOktay, Yavuz/G-4794-2015
dc.authorwosidHorvath, Rita/AAY-7042-2020
dc.contributor.authorYilmaz, E.
dc.contributor.authorSonmezler, E.
dc.contributor.authorTopf, A.
dc.contributor.authorBalaraju, S.
dc.contributor.authorYaramis, A.
dc.contributor.authorGungor, S.
dc.contributor.authorLaurie, S.
dc.date.accessioned2024-08-04T20:56:20Z
dc.date.available2024-08-04T20:56:20Z
dc.date.issued2019
dc.departmentİnönü Üniversitesien_US
dc.description51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) -- JUN 16-19, 2018 -- Milan, ITALYen_US
dc.description.abstract[Abstract Not Available]en_US
dc.description.sponsorshipEuropean Soc Human Geneten_US
dc.identifier.endpage286en_US
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.startpage285en_US
dc.identifier.urihttps://hdl.handle.net/11616/102218
dc.identifier.volume27en_US
dc.identifier.wosWOS:000489313102114en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.relation.ispartofEuropean Journal of Human Geneticsen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[No Keywords]en_US
dc.titleA novel mutation in the coiled-coil interaction domain of LAMB1 extends the molecular basis of laminin-related cortical malformation phenotypesen_US
dc.typeConference Objecten_US

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