Published in Bull World Health Organ on January 01, 1992
Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf. J Exp Med (1976) 2.89
International system for human gene nomenclature (1979) ISGN (1979). Cytogenet Cell Genet (1979) 2.58
Mapping of the structural gene for the second component of complement with respect to the human major histocompatibility complex. Am J Hum Genet (1979) 1.22
Evidence for a silent or null gene in hereditary C2 deficiency. J Immunol (1978) 1.12
C2 reference typing report. Complement Inflamm (1990) 0.88