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Uniparental isodisomy 6 associated with deficiency of the fourth component of complement.
We identified an extremely rare condition, isolated complete deficiency of the fourth component of complement, in a child with systemic lupus erythematosus. The genes for C4 are located within the major histocompatibility complex (MHC) on the short arm of chromosome 6. The patient expressed only pat...
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| Publicado no: | J Clin Invest |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
1990
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC296776/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2384609/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI114760 |
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