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

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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.kuauthorFaculty Member, Kayserili, Hülya
dc.contributor.kuauthorFaculty Member, Reversade, Bruno
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-10T00:10:57Z
dc.date.issued2017
dc.description.indexedbyWOS
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume145
dc.identifier.doi10.1016/j.mod.2017.04.025
dc.identifier.eissn1872-6356
dc.identifier.issn0925-4773
dc.identifier.quartileQ2
dc.identifier.urihttps://doi.org/10.1016/j.mod.2017.04.025
dc.identifier.urihttps://hdl.handle.net/20.500.14288/17388
dc.identifier.wos402994800100
dc.language.isoeng
dc.publisherElsevier Science Bv
dc.relation.ispartofMechanisms of Development
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
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
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