A cluster of mutations within a short triplet repeat in the C1 inhibitor gene.

Mutations in the C1 inhibitor gene that result in low functional levels of C1 inhibitor protein cause hereditary angioneurotic edema. This disease is characterized by episodic edema leading to considerable morbidity and death. Among 60 unreported kindred with the disease, four patients were discover...

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Detalles Bibliográficos

Publicado en:	Proc Natl Acad Sci U S A
Principais autores:	Bissler, J J, Cicardi, M, Donaldson, V H, Gatenby, P A, Rosen, F S, Sheffer, A L, Davis, A E
Formato:	Artigo
Idioma:	Inglês
Publicado:	National Academy of Sciences 1994
Assuntos:	Research Article
Acceso en liña:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC44865/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7937817/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.91.20.9622
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