Literature for peptidase S01.193: complement component activated C1s
(References are filtered for relevance to Mutation. To remove the filter click here. See explanation.)
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Abe,K., Endo,Y., Nakazawa,N., Kanno,K., Okubo,M., Hoshino,T. and Fujita,T.
Unique phenotypes of C1s deficiency and abnormality caused by two compound heterozygosities in a Japanese family
J Immunol182, 1681-1688. PubMed Europe PubMed M -
Amano,M.T., Ferriani,V.P., Florido,M.P., Reis,E.S., Delcolli,M.I., Azzolini,A.E., Assis-Pandochi,A.I., Sjoholm,A.G., Farah,C.S., Jensenius,J.C. and Isaac,L.
Genetic analysis of complement C1s deficiency associated with systemic lupus erythematosus highlights alternative splicing of normal C1s gene
Mol Immunol45, 1693-1702. PubMed Europe PubMed DOI M
2009
2008
