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. 2013 Mar;260(3):927-8.
doi: 10.1007/s00415-012-6830-x. Epub 2013 Jan 25.

Mutations in PDYN are not responsible for multiple system atrophy

Brent L Fogel, Cameron Baker, Andrew Curnow, Susan L Perlman, Daniel H Geschwind, Giovanni Coppola

Mutations in PDYN are not responsible for multiple system atrophy

Brent L Fogel et al. J Neurol. 2013 Mar.
No abstract available

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Conflict of interest statement

Conflict of Interest statement. None relevant to this work declared.

References

    1. Fawcett K, Mehrabian M, Liu YT, Hamed S, Elahi E, Revesz T, Koutsis G, Herscheson J, Schottlaender L, Wardle M, Morrison PJ, Morris HR, Giunti P, Wood N, Houlden H. The frequency of spinocerebellar ataxia type 23 in a UK population. J Neurol. 2012 doi: 10.1007/s00415-012-6721-1. - DOI - PubMed
    1. Bakalkin G, Watanabe H, Jezierska J, Depoorter C, Verschuuren-Bemelmans C, Bazov I, Artemenko KA, Yakovleva T, Dooijes D, Van de Warrenburg BP, Zubarev RA, Kremer B, Knapp PE, Hauser KF, Wijmenga C, Nyberg F, Sinke RJ, Verbeek DS. Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23. Am J Hum Genet. 2010;87(5):593–603. doi: 10.1016/j.ajhg.2010.10.001. S0002-9297(10)00516-1 [pii] - DOI - PMC - PubMed
    1. Schicks J, Synofzik M, Beetz C, Schiele F, Schols L. Mutations in the PDYN gene (SCA23) are not a frequent cause of dominant ataxia in Central Europe. Clin Genet. 2011;80(5):503–504. doi: 10.1111/j.1399-0004.2011.01651.x. - DOI - PubMed
    1. Fogel BL, Lee JY, Lane J, Wahnich A, Chan S, Huang A, Osborn GE, Klein E, Mamah C, Perlman S, Geschwind DH, Coppola G. Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia. Mov Disord. 2012;27(3):442–446. doi: 10.1002/mds.24064. - DOI - PMC - PubMed
    1. Gilman S, Wenning GK, Low PA, Brooks DJ, Mathias CJ, Trojanowski JQ, Wood NW, Colosimo C, Durr A, Fowler CJ, Kaufmann H, Klockgether T, Lees A, Poewe W, Quinn N, Revesz T, Robertson D, Sandroni P, Seppi K, Vidailhet M. Second consensus statement on the diagnosis of multiple system atrophy. Neurology. 2008;71(9):670–676. doi: 10.1212/01.wnl.0000324625.00404.15. 71/9/670 [pii] - DOI - PMC - PubMed

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