Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene-Reference-Cited by-同舟云学术

Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene

Published:2004-07 Issue:7 Volume:14 Page:417-420
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Bidooki Seyed,Jackson Margaret J,Johnson Margaret A,Chrzanowska-Lightowlers Zofia M.A,Taylor Robert W,Venables Graham,Lightowlers Robert N,Turnbull Douglass M,Bindoff Laurence A

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference18 articles.

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4. Cytochrome c oxidase activity in single muscle fibres: assay techniques and diagnostic applications;Johnson;Ann Neurol,1993

5. Multiple defects of the mitochondrial respiratory chain in a mitochondrial encephalopathy (MERRF): a clinical, biochemical and molecular study;Bindoff;J Neurol Sci,1991

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