SPG4‐related hereditary spastic paraplegia: frequency and mutation spectrum in Brazil. (5th September 2013)

Record Type:: Journal Article
Title:: SPG4‐related hereditary spastic paraplegia: frequency and mutation spectrum in Brazil. (5th September 2013)
Main Title:: SPG4‐related hereditary spastic paraplegia: frequency and mutation spectrum in Brazil
Authors:: França, M.C.
Dogini, D.B.
D'Abreu, A.
Teive, H.A.G.
Munhoz, R.P.
Raskin, S.
Moro, A.
Melo, C.C.
Gomes, A.P.
Saute, J.A.M.
Jardim, L.B.
Lopes‐Cendes, I.
Abstract:
Is Part Of:: Clinical genetics. Volume 86:Number 2(2014:Aug.)
Journal:: Clinical genetics
Issue:: Volume 86:Number 2(2014:Aug.)
Issue Display:: Volume 86, Issue 2 (2014)
Year:: 2014
Volume:: 86
Issue:: 2
Issue Sort Value:: 2014-0086-0002-0000
Page Start:: 194
Page End:: 196
Publication Date:: 2013-09-05
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.12252 ↗
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:: 4362.xml