A tRNAAla mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy. Issue 10 (20th October 2003)

Record Type:: Journal Article
Title:: A tRNAAla mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy. Issue 10 (20th October 2003)
Main Title:: A tRNAAla mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy
Authors:: Horváth, R
Lochmüller, H
Scharfe, C
Do, B H
Oefner, P J
Müller-Höcker, J
Schoser, B G
Pongratz, D
Auer, D P
Jaksch, M
Abstract:
Is Part Of:: Journal of medical genetics. Volume 40:Issue 10(2003)
Journal:: Journal of medical genetics
Issue:: Volume 40:Issue 10(2003)
Issue Display:: Volume 40, Issue 10 (2003)
Year:: 2003
Volume:: 40
Issue:: 10
Issue Sort Value:: 2003-0040-0010-0000
Page Start:: 752
Page End:: 757
Publication Date:: 2003-10-20
Subjects:: mitochondrial DNA mutation -- myotonic dystrophy -- ragged red fibres -- respiratory chain deficiency
Medical genetics -- Periodicals
616.042
Journal URLs:: http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jmg.40.10.752 ↗
Languages:: English
ISSNs:: 1468-6244
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:: 18592.xml