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Complement factor 2 deficiency: a clinical and serological family study.
Inherited complement deficiencies are associated with a variety of connective tissue diseases. A family with inherited deficiency of complement factor 2 (C2) is described in which two family members with homozygous C2 deficiency developed cutaneous vasculitis and sicca syndrome. The other family mem...
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| Publicado no: | Ann Rheum Dis |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
1992
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1012468/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1361318/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/ard.51.11.1254 |
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