ArticleThe Journal of experimental medicine2000

Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease.

C A Blanchong et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.