Familial intellectual disability in an Iranian family with a novel truncating mutation in CEP290. (31st October 2013)

Record Type:: Journal Article
Title:: Familial intellectual disability in an Iranian family with a novel truncating mutation in CEP290. (31st October 2013)
Main Title:: Familial intellectual disability in an Iranian family with a novel truncating mutation in CEP290
Authors:: Ghaffari, S.R.
Rafati, M.
Ghaffari, G.
Morra, M.
Tekin, M.
Abstract:
Is Part Of:: Clinical genetics. Volume 86:Number 4(2014:Oct.)
Journal:: Clinical genetics
Issue:: Volume 86:Number 4(2014:Oct.)
Issue Display:: Volume 86, Issue 4 (2014)
Year:: 2014
Volume:: 86
Issue:: 4
Issue Sort Value:: 2014-0086-0004-0000
Page Start:: 387
Page End:: 390
Publication Date:: 2013-10-31
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.12296 ↗
Languages:: English
ISSNs:: 0009-9163
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3286.287000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 4379.xml