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Publication:
A deleterious recessive mutation in NUAK2 causes absence of brain in humans

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dc.conference.dateJUN 18-22, 2017
dc.conference.locationNational University of Singapore, Singapore
dc.conference.organizer18th International Congress of Developmental Biology
dc.contributor.coauthorGhosh, Kakaly
dc.contributor.coauthorNavaratnam, Naveenan
dc.contributor.coauthorChan, Puck Wee
dc.contributor.coauthorTan, Thong Teck
dc.contributor.coauthorNg, Alvin Yu Jin
dc.contributor.coauthorTohari, Sumanty
dc.contributor.coauthorPomp, Oz
dc.contributor.coauthorVenkatesh, Byrappa
dc.contributor.coauthorAltunoglu, Umut
dc.contributor.coauthorBonnard, Carine
dc.contributor.departmentSchool of Medicine
dc.contributor.facultymemberYes
dc.contributor.kuauthorKayserili, Hülya
dc.contributor.kuauthorReversade, Bruno
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-10T00:10:57Z
dc.date.issued2017
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.openaccessNO
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.studentonlypublicationNo
dc.description.studentpublicationNo
dc.description.versionN/A
dc.identifier.WoSQuartileQ2
dc.identifier.doi10.1016/j.mod.2017.04.025
dc.identifier.eissn1872-6356
dc.identifier.embargoN/A
dc.identifier.endpageS30
dc.identifier.issn0925-4773
dc.identifier.startpageS29
dc.identifier.urihttps://doi.org/10.1016/j.mod.2017.04.025
dc.identifier.urihttps://hdl.handle.net/20.500.14288/17388
dc.identifier.volume145
dc.identifier.wos000402994800100
dc.keywordsNUAK2 mutation
dc.keywordsBrain development
dc.keywordsRecessive inheritance
dc.language.isoeng
dc.publisherElsevier
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofMechanisms of Development
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectDevelopmental biology
dc.titleA deleterious recessive mutation in NUAK2 causes absence of brain in humans
dc.typeMeeting Abstract
dspace.entity.typePublication
local.contributor.kuauthorKayserili, Hülya
local.contributor.kuauthorReversade, Bruno
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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