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

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Kesim B., Buyukozturk S., Gelincik A., Eraslan S., Uzumcu A., Mete N., ...More

27th Congress of the European-Academy-of-Allergology-and-Clinical-Immunology, Barcelona, Spain, 7 - 11 June 2008, vol.63, pp.340, (Summary Text)

• Publication Type: Conference Paper / Summary Text
• Volume: 63
• City: Barcelona
• Country: Spain
• Page Numbers: pp.340
• Istanbul University Affiliated: Yes