Phenotypic diversity in a Turkish family with hereditary angioedema type 1 due to a novel C1INH gene mutation and outcomes of long term treatments | AVESİS

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Phenotypic diversity in a Turkish family with hereditary angioedema type 1 due to a novel C1INH gene mutation and outcomes of long term treatments

Akoğlu G., Emre S., Kesim B., YILDIZ G., Metin A.

23rd EADV Congress, Amsterdam, Netherlands, 8 - 12 October 2014, pp.132

Publication Type: Conference Paper / Full Text
City: Amsterdam
Country: Netherlands
Page Numbers: pp.132