TY  - RPRT
TI  - Hereditary C2 deficiency associated with common variable immunodeficiency.
AU  - M Seligmann
AU  - J C Brouet
AU  - M Sasportes
PY  - 1979
DO  - 10.7326/0003-4819-91-2-216
UR  - https://pubmed.ncbi.nlm.nih.gov/313733/
ID  - 313733
ER  -