Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome. Issue 2 (2nd February 2005)

Record Type:: Journal Article
Title:: Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome. Issue 2 (2nd February 2005)
Main Title:: Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome
Authors:: Amir, R E
Fang, P
Yu, Z
Glaze, D G
Percy, A K
Zoghbi, H Y
Roa, B B
Van den Veyver, I B
Abstract:
Is Part Of:: Journal of medical genetics. Volume 42:Issue 2(2005)
Journal:: Journal of medical genetics
Issue:: Volume 42:Issue 2(2005)
Issue Display:: Volume 42, Issue 2 (2005)
Year:: 2005
Volume:: 42
Issue:: 2
Issue Sort Value:: 2005-0042-0002-0000
Page Start:: e15
Page End:: e15
Publication Date:: 2005-02-02
Subjects:: AR, androgen receptor -- RTT, Rett syndrome -- XCI, X chromosome inactivation
Methyl-CpG-binding protein -- Rett syndrome -- X chromosome inactivation
Medical genetics -- Periodicals
616.042
Journal URLs:: http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jmg.2004.026161 ↗
Languages:: English
ISSNs:: 1468-6244
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 17870.xml