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83 Hereditary Angioedema and Normal C1-Inhibitor (HAE TYPE III): A Novel Mutation in the Coagulation Factor 12 Gene
BACKGROUND: Hereditary angioedema with normal C1-inhibitor and mutations in the coagulation factor 12 gene is a recently described disease entity that occurs predominantly in women. Up to date, 2 different missense mutations of codon p.Thr328* in the coagulation factor 12 gene have been reported, co...
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| Auteurs principaux: | , , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
World Allergy Organization Journal
2012
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3512582/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/01.WOX.0000411828.92623.28 |
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