dc.contributor.author | Ross, PD | en_US |
dc.contributor.author | Guy, J | en_US |
dc.contributor.author | Selfridge, J | en_US |
dc.contributor.author | Kamal, B | en_US |
dc.contributor.author | Bahey, N | en_US |
dc.contributor.author | Tanner, KE | en_US |
dc.contributor.author | Gillingwater, TH | en_US |
dc.contributor.author | Jones, RA | en_US |
dc.contributor.author | Loughrey, CM | en_US |
dc.contributor.author | McCarroll, CS | en_US |
dc.contributor.author | Bailey, MES | en_US |
dc.contributor.author | Bird, A | en_US |
dc.contributor.author | Cobb, S | en_US |
dc.date.accessioned | 2018-11-21T13:36:29Z | |
dc.date.available | 2016-08-03 | en_US |
dc.date.issued | 2016-10-15 | en_US |
dc.date.submitted | 2018-11-21T11:44:52.112Z | |
dc.identifier.issn | 0964-6906 | en_US |
dc.identifier.other | 10.1093/hmg/ddw269 | |
dc.identifier.uri | http://qmro.qmul.ac.uk/xmlui/handle/123456789/52603 | |
dc.description | This 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/ddw269 | en_US |
dc.description.sponsorship | Work 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.extent | 4389 - 4404 | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | HUMAN MOLECULAR GENETICS | en_US |
dc.rights | Creative Commons Attribution License | |
dc.title | Exclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypes | en_US |
dc.type | Article | |
dc.rights.holder | The Author 2016 | |
dc.identifier.doi | 10.1093/hmg/ddw269 | en_US |
pubs.author-url | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000395809100003&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6a | en_US |
pubs.issue | 20 | en_US |
pubs.notes | No embargo | en_US |
pubs.notes | Open Access publication. | en_US |
pubs.publication-status | Published | en_US |
pubs.volume | 25 | en_US |