Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia. Issue 6 (1st June 2003)

Record Type:: Journal Article
Title:: Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia. Issue 6 (1st June 2003)
Main Title:: Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia
Authors:: Philip, N
Chabrol, B
Lossi, A-M
Cardoso, C
Guerrini, R
Dobyns, W B
Raybaud, C
Villard, L
Abstract:
Is Part Of:: Journal of medical genetics. Volume 40:Issue 6(2003)
Journal:: Journal of medical genetics
Issue:: Volume 40:Issue 6(2003)
Issue Display:: Volume 40, Issue 6 (2003)
Year:: 2003
Volume:: 40
Issue:: 6
Issue Sort Value:: 2003-0040-0006-0000
Page Start:: 441
Page End:: 446
Publication Date:: 2003-06-01
Subjects:: brain development -- cerebellum -- mental retardation -- oligophrenin-1
Medical genetics -- Periodicals
616.042
Journal URLs:: http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jmg.40.6.441 ↗
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:: 17973.xml