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Journal Abstract Search

231 related items for PubMed ID: 15781840

  • 1. Nonsense mutations in mitochondrial DNA associated with myalgia and exercise intolerance.
    Pulkes T, Liolitsa D, Wills AJ, Hargreaves I, Heales S, Hanna MG.
    Neurology; 2005 Mar 22; 64(6):1091-2. PubMed ID: 15781840
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  • 7. TPM3 mutation in one of the original cases of cap disease.
    Ohlsson M, Fidzianska A, Tajsharghi H, Oldfors A.
    Neurology; 2009 Jun 02; 72(22):1961-3. PubMed ID: 19487656
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  • 10. A novel homozygous RRM2B missense mutation in association with severe mtDNA depletion.
    Kollberg G, Darin N, Benan K, Moslemi AR, Lindal S, Tulinius M, Oldfors A, Holme E.
    Neuromuscul Disord; 2009 Feb 02; 19(2):147-50. PubMed ID: 19138848
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  • 11. Symptomatic dysferlin gene mutation carriers: characterization of two cases.
    Illa I, De Luna N, Domínguez-Perles R, Rojas-García R, Paradas C, Palmer J, Márquez C, Gallano P, Gallardo E.
    Neurology; 2007 Apr 17; 68(16):1284-9. PubMed ID: 17287450
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