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pro vyhledávání: '"Ulivieri, Mf"'
Autor:
Falchetti, A, Di Stefano, M, Marini, F, Ortolani, S, Ulivieri, Mf, Bergui, S, Masi, L, Cepollaro, C, Benucci, M, Di Munno, O, Rossini, Maurizio, Adami, Silvano, Del Puente, A, Isaia, G, Torricelli, F, Brandi, Ml, Genepage, Project
Families affected by Paget's disease of bone frequently harbor mutations in the SQSTM1/p62 gene. In this multicentric study we collected 345 sporadic and 12 familial PDB cases throughout Italy, identifying 12 different mutations, 5 of which are newly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e25c1d58f3ee451f6bc81dbb50dcbf50
http://hdl.handle.net/11562/340244
http://hdl.handle.net/11562/340244
Autor:
Falchetti A; Department of Internal Medicine, University of Florence, Florence, Italy. a.falchetti@dmi.unifi.it, Di Stefano M, Marini F, Ortolani S, Ulivieri MF, Bergui S, Masi L, Cepollaro C, Benucci M, Di Munno O, Rossini M, Adami S, Del Puente A, Isaia G, Torricelli F, Brandi ML
Publikováno v:
Calcified tissue international [Calcif Tissue Int] 2009 Jan; Vol. 84 (1), pp. 20-37. Date of Electronic Publication: 2008 Dec 09.
