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Panminerva Medica 2011 March;53(1):71-2

lingua: Inglese

Detection of Exon 8 mutations in sqstm1/p62 gene by mutation-specific restriction enzyme digestion: a sensitive screening for Paget disease of bone

Gallone S. 1, Di Stefano M. 2, Rainero I. 1, Fenoglio P. 1, Gravante E. 1, Incardona S. 1, Acutis P. L. 3, Maniaci M. G. 3, Isaia G. C. 2, Pinessi L. 1

1 Neurology Unit, Department of Neuroscience, University of Turin, Turin, Italy;
2 Department of Internal Medicine, University of Turin, Turin, Italy;
3 CEA, Istituto Zooprofilattico, del Piemonte, Liguria e Valle d’Aosta, Turin, Italy


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sgallone@molinette.piemonte.it