Corpus callosum thinning in autosomal dominant hereditary spastic paraplegia associated with a novel TUBβ4A mutation. Issue 4 (28th July 2020)

Record Type:: Journal Article
Title:: Corpus callosum thinning in autosomal dominant hereditary spastic paraplegia associated with a novel TUBβ4A mutation. Issue 4 (28th July 2020)
Main Title:: Corpus callosum thinning in autosomal dominant hereditary spastic paraplegia associated with a novel TUBβ4A mutation
Authors:: Lamartine S. Monteiro, Marta
Vandernoot, Isabelle
Desmyter, Laurence
Wermenbol, Vanessa
Naeije, Gilles
Remiche, Gauthier
Abstract:: Abstract : Siblings with hereditary spastic paraplegia and corpus callosum thinning associated with a novel TUBβ4A mutation.
Is Part Of:: Clinical genetics. Volume 98:Issue 4(2020)
Journal:: Clinical genetics
Issue:: Volume 98:Issue 4(2020)
Issue Display:: Volume 98, Issue 4 (2020)
Year:: 2020
Volume:: 98
Issue:: 4
Issue Sort Value:: 2020-0098-0004-0000
Page Start:: 416
Page End:: 417
Publication Date:: 2020-07-28
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.13809 ↗
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:: 14280.xml