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A combined omic analysis revealed autism-linked NLGN3 as a new candidate gene associated to GnRH neuron development and disease

dc.contributor.authorOleari, Ren_US
dc.contributor.authorLettieri, Aen_US
dc.contributor.authorManzini, Sen_US
dc.contributor.authorPaganoni, AJJen_US
dc.contributor.authorGrazioli, Pen_US
dc.contributor.authorBusnelli, Men_US
dc.contributor.authorStorr, HLen_US
dc.contributor.authorMassa, Ven_US
dc.contributor.authorHoward, SRen_US
dc.contributor.authorCariboni, Aen_US
dc.date.accessioned2022-06-09T14:47:35Z
dc.date.issued2022en_US
dc.identifier.issn1018-4813en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/78824
dc.format.extent34 - 34en_US
dc.titleA combined omic analysis revealed autism-linked NLGN3 as a new candidate gene associated to GnRH neuron development and diseaseen_US
dc.typeConference Proceeding
pubs.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000779367700094&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issueSUPPL 1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume30en_US
qmul.funderDisorders of human pubertal timing::Wellcome Trusten_US
qmul.funderDisorders of human pubertal timing::Wellcome Trusten_US


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