Molecular basis of hereditary C3 deficiency.

Hereditary deficiency of complement component C3 in a 10-yr-old boy was studied. C3 could not be detected by RIA of serum from the patient. Segregation of C3 S and C3 F allotypes within the family confirmed the presence of a null gene for C3, for which the patient was homozygous. 30 exons have been...

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Bibliografiske detaljer

Udgivet i:	J Clin Invest
Principais autores:	Botto, M, Fong, K Y, So, A K, Rudge, A, Walport, M J
Format:	Artigo
Sprog:	Inglês
Udgivet:	American Society for Clinical Investigation 1990
Fag:	Research Article
Online adgang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC296845/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2212005/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI114821
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