Akoğlu, G. Et Al. 2014. Phenotypic diversity in a Turkish family with hereditary angioedema type 1 due to a novel C1INH gene mutation and outcomes of long term treatments. 23rd EADV Congress , (Amsterdam, Netherlands), 132.

Akoğlu, G., Emre, S., Kesim, B., YILDIZ, G., & Metin, A., (2014). Phenotypic diversity in a Turkish family with hereditary angioedema type 1 due to a novel C1INH gene mutation and outcomes of long term treatments . 23rd EADV Congress (pp.132). Amsterdam, Netherlands

Akoğlu, Gülşen Et Al. "Phenotypic diversity in a Turkish family with hereditary angioedema type 1 due to a novel C1INH gene mutation and outcomes of long term treatments," 23rd EADV Congress, Amsterdam, Netherlands, 2014

Akoğlu, Gülşen Et Al. "Phenotypic diversity in a Turkish family with hereditary angioedema type 1 due to a novel C1INH gene mutation and outcomes of long term treatments." 23rd EADV Congress , Amsterdam, Netherlands, pp.132, 2014

Akoğlu, G. Et Al. (2014) . "Phenotypic diversity in a Turkish family with hereditary angioedema type 1 due to a novel C1INH gene mutation and outcomes of long term treatments." 23rd EADV Congress , Amsterdam, Netherlands, p.132.

@conferencepaper{conferencepaper, author={Gülşen Akoğlu Et Al. }, title={Phenotypic diversity in a Turkish family with hereditary angioedema type 1 due to a novel C1INH gene mutation and outcomes of long term treatments}, congress name={23rd EADV Congress}, city={Amsterdam}, country={Netherlands}, year={2014}, pages={132} }