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Giordano C, Sebastiani M, De Giorgio R, et al. 
Gastrointestinal dysmotility in mitochondrial neurogastrointestinal encephalomyopathy is caused by mitochondrial DNA depletion. [Journal Article, Research Support, Non-U.S. Gov't]
Am J Pathol 2008 Oct; 173(4):1120-8.
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Giordano C, Sebastiani M, Plazzi G, et al. 
Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine. [Case Reports, Journal Article]
Gastroenterology 2006 Mar; 130(3):893-901.
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Hirano M, Nishigaki Y, Martí R 
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomes. [Journal Article, Review]
Neurologist 2004 Jan; 10(1):8-17.
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Nishino I, Spinazzola A, Papadimitriou A, et al. 
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutations. [Journal Article]
Ann Neurol 2000 Jun; 47(6):792-800.
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Hirano M, Lagier-Tourenne C, Valentino ML, et al. 
Thymidine phosphorylase mutations cause instability of mitochondrial DNA. [Journal Article]
Gene 2005 Jul 18.:152-6.
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Slama A, Lacroix C, Plante-Bordeneuve V, et al. 
Thymidine phosphorylase gene mutations in patients with mitochondrial neurogastrointestinal encephalomyopathy syndrome. [Journal Article]
Mol Genet Metab 2005 Apr; 84(4):326-31.
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Valentino ML, Martı R, Tadesse S, et al. 
Thymidine and deoxyuridine accumulate in tissues of patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE). [JOURNAL ARTICLE]
FEBS Lett 2007 Jun 27.
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Nishigaki Y, Marti R, Hirano M 
ND5 is a hot-spot for multiple atypical mitochondrial DNA deletions in mitochondrial neurogastrointestinal encephalomyopathy. [Journal Article]
Hum Mol Genet 2004 Jan 1; 13(1):91-101.
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Honzík T, Tesarová M, Hansíková H, et al. 
[Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)] [Journal Article]
Cas Lek Cesk 2006; 145(8):665-70.
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