Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum. (March 2014)

Record Type:: Journal Article
Title:: Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum. (March 2014)
Main Title:: Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum
Authors:: Magariello, A.
Citrigno, L.
Zuchner, S.
Gonzalez, M.
Patitucci, A.
Sofia, V.
Conforti, F. L.
Pappalardo, I.
Mazzei, R.
Ungaro, C.
Zappia, M.
Muglia, M.
Abstract:
Is Part Of:: European journal of neurology. Volume 21:Number 3(2014:Mar.)
Journal:: European journal of neurology
Issue:: Volume 21:Number 3(2014:Mar.)
Issue Display:: Volume 21, Issue 3 (2014)
Year:: 2014
Volume:: 21
Issue:: 3
Issue Sort Value:: 2014-0021-0003-0000
Page Start:: e25
Page End:: e26
Publication Date:: 2014-03
Subjects:: Neurology -- Periodicals
Nervous system -- Diseases -- Periodicals
616.8
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1468-1331 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/ene.12305 ↗
Languages:: English
ISSNs:: 1351-5101
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3829.731680
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 3622.xml