A case of Buerger's disease associated with MTHFR C677T mutation homozygosity: a possible therapeutic support
P. Di Micco, A. Niglio, O. Scudiero, B. Bonamassa, I. Martinelli, R. Di Fiore, G. Castaldo, F. SalvatoreVolume:
14
Year:
2004
Language:
english
DOI:
10.1016/s0939-4753(04)80009-7
File:
PDF, 187 KB
english, 2004