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Combined genetic deficiency of C6 and C7 in man.

By routine screening of sera, a subject was discovered who showed a sub-total deficiency of C6 and C7. No clinical disease was associated with this deficiency which was transmitted through the subject's family as a single genetic characteristic, the C6 deficiency being associated with a silent...

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Библиографические подробности
Главные авторы: Lachmann, P J, Hobart, M J, Woo, P
Формат: Artigo
Язык:Inglês
Опубликовано: 1978
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Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC1537564/
https://ncbi.nlm.nih.gov/pubmed/102474
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