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
Jazyk: angličtina
Zdroj: Panminerva medica [Panminerva Med] 2011 Mar; Vol. 53 (1), pp. 71-2.
Databáze: MEDLINE