Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia. (27th November 2013)

Record Type:: Journal Article
Title:: Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia. (27th November 2013)
Main Title:: Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia
Authors:: Wakil, S.M.
Monies, D.M.
Ramzan, K.
Hagos, S.
Bastaki, L.
Meyer, B.F.
Bohlega, S.
Abstract:
Is Part Of:: Clinical genetics. Volume 86:Number 5(2014:Nov.)
Journal:: Clinical genetics
Issue:: Volume 86:Number 5(2014:Nov.)
Issue Display:: Volume 86, Issue 5 (2014)
Year:: 2014
Volume:: 86
Issue:: 5
Issue Sort Value:: 2014-0086-0005-0000
Page Start:: 500
Page End:: 501
Publication Date:: 2013-11-27
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.12312 ↗
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:: 4237.xml