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A Missense Mutation of the Plasminogen Gene in a Japanese Family with Hereditary Angioedema with Normal C1 Inhibitor: Third Family Survey in Asia
Hereditary angioedema (HAE) is a life-threatening disease associated with recurrent episodes of subcutaneous and mucosal swelling, painful abdominal cramping, and asphyxiation. HAE has long been thought to be caused by genetic defects of C1 inhibitors (C1-INH). Recently, HAE with a normal C1 inhibit...
Autores principales: | Yakushiji, Hiromasa, Yamagami, Keiko, Hashimura, Chinami, Iwasaki, Hiromi, Horiuchi, Takahiko |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Internal Medicine
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372273/ https://www.ncbi.nlm.nih.gov/pubmed/36418094 http://dx.doi.org/10.2169/internalmedicine.0645-22 |
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