bone and mineral research
Haplotype analysis of two pairs of unrelated Italian families affected by Paget's disease of bone, exhibiting different geographical origins and two different mutations of p62/sequestosomel gene, supports the evidence for common founders / A. Falchetti;M. D. Stefano;F. Marini;L. Masi;F. Giusti;C. Cepollaro;E. Luzi;V. Martineti;C. Mavilia;D. Strigoli;S. Bergui;G. Isaia;M. L. Brandi. - STAMPA. - 21:(2006), pp. 437-437. (Intervento presentato al convegno 28th Annual Meeting of the American-Society-for-Bone-and-Mineral-Research nel 2006-sep).
Haplotype analysis of two pairs of unrelated Italian families affected by Paget's disease of bone, exhibiting different geographical origins and two different mutations of p62/sequestosomel gene, supports the evidence for common founders.
FALCHETTI, ALBERTO;MARINI, FRANCESCA;GIUSTI, FRANCESCA;CEPOLLARO, CHIARA;LUZI, ETTORE;MARTINETI, VALENTINA;MAVILIA, CARMELO;STRIGOLI, DEBORA;BRANDI, MARIA LUISA
2006
Abstract
bone and mineral research
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