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dc.contributor.authorRoss, PDen_US
dc.contributor.authorGuy, Jen_US
dc.contributor.authorSelfridge, Jen_US
dc.contributor.authorKamal, Ben_US
dc.contributor.authorBahey, Nen_US
dc.contributor.authorTanner, KEen_US
dc.contributor.authorGillingwater, THen_US
dc.contributor.authorJones, RAen_US
dc.contributor.authorLoughrey, CMen_US
dc.contributor.authorMcCarroll, CSen_US
dc.contributor.authorBailey, MESen_US
dc.contributor.authorBird, Aen_US
dc.contributor.authorCobb, Sen_US
dc.date.accessioned2018-11-21T13:36:29Z
dc.date.available2016-08-03en_US
dc.date.issued2016-10-15en_US
dc.date.submitted2018-11-21T11:44:52.112Z
dc.identifier.issn0964-6906en_US
dc.identifier.other10.1093/hmg/ddw269
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/52603
dc.descriptionThis is a pre-copyedited, author-produced version of an article accepted for publication in Human Molecular Genetics following peer review. The version of record Ross, P. D., et al. (2016). "Exclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypes." Human Molecular Genetics 25(20): 4389-4404.] is available online at: https://doi.org/10.1093/hmg/ddw269en_US
dc.description.sponsorshipWork in SC’s laboratory was supported by the Biotechnology and Biological Sciences Research Council (PhD studentship for PDR), a consortium grant from the Rett Syndrome Research Trust, the Chief Scientist Office (Scottish Executive Health Department) [grant ETM/334], RS Macdonald Charitable Trust, Rosetrees Trust [grant M530], and the Rett Syndrome Association Scotland. Work in AB’s laboratory was supported by a Consortium Grant from the Rett Syndrome Research Trust, by Wellcome Trust programme grant [091580] and by Wellcome Trust Centre Core Grant [092076]. Funding to pay the Open Access publication charges for this article was provided by the Scottish Executive Health Department.en_US
dc.format.extent4389 - 4404en_US
dc.language.isoenen_US
dc.relation.ispartofHUMAN MOLECULAR GENETICSen_US
dc.rightsCreative Commons Attribution License
dc.titleExclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypesen_US
dc.typeArticle
dc.rights.holderThe Author 2016
dc.identifier.doi10.1093/hmg/ddw269en_US
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000395809100003&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issue20en_US
pubs.notesNo embargoen_US
pubs.notesOpen Access publication.en_US
pubs.publication-statusPublisheden_US
pubs.volume25en_US


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