TREX1 mutations are not associated with sporadic inclusion body myositis

Autor: Fieke M.E. Cox, Jan J.G.M. Verschuuren, Umesh A. Badrising, Egbert Bakker, E. M. J. Boon, C. A. C. Van Der Lans

Publikováno v: European Journal of Neurology, 17(8), 1108-1109
European Journal of Neurology, 17(8), 1108-1109. Wiley-Blackwell
Cox, F M, Boon, E M J, Van Der Lans, C A C, Bakker, E, Verschuuren, J J G M & Badrising, U A 2010, ' TREX1 mutations are not associated with sporadic inclusion body myositis ', European Journal of Neurology, vol. 17, no. 8, pp. 1108-1109 . https://doi.org/10.1111/j.1468-1331.2010.02964.x

Background: Sporadic inclusion body myositis (sIBM) is the most frequent acquired myopathy above the age of fifty. The exact mechanism causing this disease is not known, but immune-mediated features are prominent and are probably to play a role in it

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1fe5e5fda8857826340d9c7c96e7c2a
https://hdl.handle.net/1887/100753