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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.
Blanchong CA, Zhou B, Rupert KL, Chung EK, Jones KN, Sotos JF, Zipf WB, Rennebohm RM, Yung Yu C. Blanchong CA, et al. J Exp Med. 2000 Jun 19;191(12):2183-96. doi: 10.1084/jem.191.12.2183. J Exp Med. 2000. PMID: 10859342 Free PMC article.