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. (28th Annual Meeting of the American-Society-for-Bone-and-Mineral-Research 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
File in questo prodotto:
Non ci sono file associati a questo prodotto.
I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
