B. Kesim Et Al. , "Analysis of genetic mutations in patients with hereditary angioedema (HAE) type I identified one family with novel homozygous mutation indicating rare instance of autosomal recessive inheritance," 27th Congress of the European-Academy-of-Allergology-and-Clinical-Immunology , vol.63, Barcelona, Spain, pp.340, 2008
Kesim, B. Et Al. 2008. Analysis of genetic mutations in patients with hereditary angioedema (HAE) type I identified one family with novel homozygous mutation indicating rare instance of autosomal recessive inheritance. 27th Congress of the European-Academy-of-Allergology-and-Clinical-Immunology , (Barcelona, Spain), 340.
Kesim, B., Buyukozturk, S., Gelincik, A., Eraslan, S., Uzumcu, A., Mete, N., ... Sin, A.(2008). Analysis of genetic mutations in patients with hereditary angioedema (HAE) type I identified one family with novel homozygous mutation indicating rare instance of autosomal recessive inheritance . 27th Congress of the European-Academy-of-Allergology-and-Clinical-Immunology (pp.340). Barcelona, Spain
Kesim, B. Et Al. "Analysis of genetic mutations in patients with hereditary angioedema (HAE) type I identified one family with novel homozygous mutation indicating rare instance of autosomal recessive inheritance," 27th Congress of the European-Academy-of-Allergology-and-Clinical-Immunology, Barcelona, Spain, 2008
Kesim, B. Et Al. "Analysis of genetic mutations in patients with hereditary angioedema (HAE) type I identified one family with novel homozygous mutation indicating rare instance of autosomal recessive inheritance." 27th Congress of the European-Academy-of-Allergology-and-Clinical-Immunology , Barcelona, Spain, pp.340, 2008
Kesim, B. Et Al. (2008) . "Analysis of genetic mutations in patients with hereditary angioedema (HAE) type I identified one family with novel homozygous mutation indicating rare instance of autosomal recessive inheritance." 27th Congress of the European-Academy-of-Allergology-and-Clinical-Immunology , Barcelona, Spain, p.340.
@conferencepaper{conferencepaper, author={B. Kesim Et Al. }, title={Analysis of genetic mutations in patients with hereditary angioedema (HAE) type I identified one family with novel homozygous mutation indicating rare instance of autosomal recessive inheritance}, congress name={27th Congress of the European-Academy-of-Allergology-and-Clinical-Immunology}, city={Barcelona}, country={Spain}, year={2008}, pages={340} }