Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNAGly (MT-TG) variant. (April 2020)

Record Type:
Journal Article
Title:
Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNAGly (MT-TG) variant. (April 2020)
Main Title:
Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNAGly (MT-TG) variant
Authors:
Poole, Olivia V.
Horga, Alejandro
Hardy, Steven A.
Bugiardini, Enrico
Woodward, Cathy E.
Hargreaves, Iain P.
Merve, Ashirwad
Quinlivan, Rosaline
Taylor, Robert W.
Hanna, Michael G.
Pitceathly, Robert D.S.
Abstract:
Is Part Of:
Neurology. Volume 6:Number 2(2020)
Journal:
Neurology
Issue:
Volume 6:Number 2(2020)
Issue Display:
Volume 6, Issue 2 (2020)
Year:
2020
Volume:
6
Issue:
2
Issue Sort Value:
2020-0006-0002-0000
Page Start:
Page End:
Publication Date:
2020-04
Subjects:
Neurogenetics -- Periodicals
616.80442
Journal URLs:
http://ng.neurology.org/ ↗
http://journals.lww.com/pages/default.aspx ↗
DOI:
10.1212/NXG.0000000000000413 ↗
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
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Ingest File:
13748.xml