@article{2206078c1be04f9695ef7a75acbc52cf,
title = "Mitochondrial DNA depletion syndromes - Many genes, common mechanisms",
keywords = "Mitochondrial DNA, Mitochondrial DNA depletion syndrome, Encephalopathy, Hepatoencephalopathy, Leigh syndrome, Alpers syndrome, PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, ONSET SPINOCEREBELLAR ATAXIA, NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY MNGIE, RECESSIVE TWINKLE MUTATIONS, POLYMERASE-GAMMA MUTATIONS, SUCCINYL-COA SYNTHETASES, MTDNA DEPLETION, THYMIDINE KINASE, DEOXYGUANOSINE KINASE, POLG1 MUTATIONS, 312 Clinical medicine",
author = "Anu Wartiovaara and Pirjo Isohanni",
year = "2010",
doi = "10.1016/j.nmd.2010.03.017",
language = "English",
volume = "20",
pages = "429--437",
journal = "Neuromuscular Disorders",
issn = "0960-8966",
publisher = "Elsevier Scientific Publ. Co",
number = "7",
}