CCDC82 frameshift mutation associated with intellectual disability, spastic paraparesis, and dysmorphic features. Issue 1 (3rd April 2022)

Record Type:: Journal Article
Title:: CCDC82 frameshift mutation associated with intellectual disability, spastic paraparesis, and dysmorphic features. Issue 1 (3rd April 2022)
Main Title:: CCDC82 frameshift mutation associated with intellectual disability, spastic paraparesis, and dysmorphic features
Authors:: Bauer, Gregor
Buchert, Rebecca
Haack, Tobias B.
Harting, Inga
Gutschalk, Alexander
Abstract:: Abstract :
Is Part Of:: Clinical genetics. Volume 102:Issue 1(2022)
Journal:: Clinical genetics
Issue:: Volume 102:Issue 1(2022)
Issue Display:: Volume 102, Issue 1 (2022)
Year:: 2022
Volume:: 102
Issue:: 1
Issue Sort Value:: 2022-0102-0001-0000
Page Start:: 80
Page End:: 81
Publication Date:: 2022-04-03
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.14135 ↗
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:: 21830.xml