Detection of Exon 8 mutations in sqstm1/p62 gene by mutation-specific restriction enzyme digestion: a sensitive screening for Paget disease of bone.
Autor: | Gallone S, Di Stefano M, Rainero I, Fenoglio P, Gravante E, Incardona S, Acutis PL, Maniaci MG, Isaia GC, Pinessi L |
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Jazyk: | angličtina |
Zdroj: | Panminerva medica [Panminerva Med] 2011 Mar; Vol. 53 (1), pp. 71-2. |
Databáze: | MEDLINE |
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