Functional characterisation of MeCP2 mutations found in male patients with X linked mental retardation. Issue 2 (1st February 2002)

Record Type:: Journal Article
Title:: Functional characterisation of MeCP2 mutations found in male patients with X linked mental retardation. Issue 2 (1st February 2002)
Main Title:: Functional characterisation of MeCP2 mutations found in male patients with X linked mental retardation
Authors:: Kudo, S
Nomura, Y
Segawa, M
Fujita, N
Nakao, M
Hammer, S
Schanen, C
Terai, I
Tamura, M
Abstract:
Is Part Of:: Journal of medical genetics. Volume 39:Issue 2(2002)
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 2(2002)
Issue Display:: Volume 39, Issue 2 (2002)
Year:: 2002
Volume:: 39
Issue:: 2
Issue Sort Value:: 2002-0039-0002-0000
Page Start:: 132
Page End:: 136
Publication Date:: 2002-02-01
Subjects:: Rett syndrome -- MeCP2 -- X linked mental retardation
Medical genetics -- Periodicals
616.042
Journal URLs:: http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jmg.39.2.132 ↗
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:: 18279.xml