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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. Among authors: chung ek. 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.
Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European Americans.
Yang Y, Chung EK, Wu YL, Savelli SL, Nagaraja HN, Zhou B, Hebert M, Jones KN, Shu Y, Kitzmiller K, Blanchong CA, McBride KL, Higgins GC, Rennebohm RM, Rice RR, Hackshaw KV, Roubey RA, Grossman JM, Tsao BP, Birmingham DJ, Rovin BH, Hebert LA, Yu CY. Yang Y, et al. Among authors: chung ek. Am J Hum Genet. 2007 Jun;80(6):1037-54. doi: 10.1086/518257. Epub 2007 Apr 26. Am J Hum Genet. 2007. PMID: 17503323 Free PMC article.
349 results