Mitochondrial DNA disease—molecular insights and potential routes to a cure-Reference-Cited by-同舟云学术

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Mitochondrial DNA disease—molecular insights and potential routes to a cure

Published:2014-07 Issue:1 Volume:325 Page:38-43
ISSN:0014-4827
Container-title:Experimental Cell Research
language:en
Short-container-title:Experimental Cell Research

Author:

Russell Oliver,Turnbull Doug

Funder

Newcastle University Centre for Brain Ageing and Vitality

Newcastle upon Tyne Hospitals NHS Foundation Trust

MRC Centre for Neuromuscular Disease

Wellcome Trust Centre for Mitochondrial Research

The Lily Foundation

UK NHS Specialist Commissioners “Rare Mitochondrial Disorders of Adults and Children” Service

Publisher

Elsevier BV

Subject

Cell Biology

Reference40 articles.

1. Coupling of phosphorylation to electron and hydrogen transfer by a chemi-osmotic type of mechanism;Mitchell;Nature,1961

2. Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature;Fukuhara;J. Neurol. Sci.,1980

3. Spontaneous Kearns–Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy;Shoffner;Proc. Natl. Acad. Sci. USA,1989

4. Sequence and organization of the human mitochondrial genome;Anderson;Nature,1981

5. Deletions of muscle mitochondrial-DNA in patients with mitochondrial myopathies;Holt;Nature,1988

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