First report of a FXII gene mutation in a Brazilian family with hereditary angio-oedema with normal C1 inhibitor
Stieber, C. ; Grumach, A.S. ; Cordeiro, E. ; Constantino-Silva, R.N. ; Barth, S. ; Hoffmann, P. ; Pesquero, J.B. ; Renné, T. ; Nöthen, M.M. ; Cichon, S.
British journal of dermatology (1951), 2015-10, Vol.173 (4), p.1102-1104 [Periódico revisado por pares]England: Blackwell Publishing Ltd
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