Hereditary deficiency of the seventh component of complement.
Deficiency of the seventh component of complement has been found in the serum of a 42-yr-old Caucasian woman who has Raynaud's phenomenon, sclerodactyly, and telangiectasia. Partial deficiency was found in the serum of the patient's parents and children, indicating a pattern of inheritance of autoso...
保存先:
| 出版年: | J Clin Invest |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Society for Clinical Investigation
1975
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC301946/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1099121/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI108170 |
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