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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, October 2015, Vol.173(4), pp.1102-1104 [Peer Reviewed Journal]

John Wiley & Sons, Inc.

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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

The British journal of dermatology, October 2015, Vol.173(4), pp.1102-4 [Peer Reviewed Journal]

MEDLINE/PubMed (U.S. National Library of Medicine)

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First report of a FXII gene mutation in a Brazilian family with hereditary angio-oedema with normal C1 inhibitor
Material Type:
Article
Add to e-Shelf

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, 10/2015, Vol.173(4), pp.1102-1104 [Peer Reviewed Journal]

Wiley (via CrossRef)

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3 Results  for Everything (Includes Articles)

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