Biallelic LINE insertion mutation in HACD1 causing congenital myopathy. (June 2020)

Record Type:: Journal Article
Title:: Biallelic LINE insertion mutation in HACD1 causing congenital myopathy. (June 2020)
Main Title:: Biallelic LINE insertion mutation in HACD1 causing congenital myopathy
Authors:: Al Amrani, Fatema
Gorodetsky, Carolina
Hazrati, Lili-Naz
Amburgey, Kimberly
Gonorazky, Hernan D.
Dowling, James J.
Abstract:
Is Part Of:: Neurology. Volume 6:Number 3(2020)
Journal:: Neurology
Issue:: Volume 6:Number 3(2020)
Issue Display:: Volume 6, Issue 3 (2020)
Year:: 2020
Volume:: 6
Issue:: 3
Issue Sort Value:: 2020-0006-0003-0000
Page Start:
Page End:
Publication Date:: 2020-06
Subjects:: Neurogenetics -- Periodicals
616.80442
Journal URLs:: http://ng.neurology.org/ ↗
http://journals.lww.com/pages/default.aspx ↗
DOI:: 10.1212/NXG.0000000000000423 ↗
Languages:: English
ISSNs:: 2376-7839
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 13761.xml