Intrafamilial variable spastic paraplegia/ataxia/ALS phenotype linked to a novel KIF5A mutation. Issue 3 (8th July 2019)

Record Type:: Journal Article
Title:: Intrafamilial variable spastic paraplegia/ataxia/ALS phenotype linked to a novel KIF5A mutation. Issue 3 (8th July 2019)
Main Title:: Intrafamilial variable spastic paraplegia/ataxia/ALS phenotype linked to a novel KIF5A mutation
Authors:: Faruq, Mohammed
Kumar, Deepak
Wadhwa, Saruchi
Shamim, Uzma
Mathur, Aradhana
Parveen, Shaista
Garg, Ajay
Srivastava, Achal K.
Abstract:
Is Part Of:: Clinical genetics. Volume 96:Issue 3(2019)
Journal:: Clinical genetics
Issue:: Volume 96:Issue 3(2019)
Issue Display:: Volume 96, Issue 3 (2019)
Year:: 2019
Volume:: 96
Issue:: 3
Issue Sort Value:: 2019-0096-0003-0000
Page Start:: 271
Page End:: 273
Publication Date:: 2019-07-08
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.13585 ↗
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
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Ingest File:: 16298.xml