TY - JOUR
T1 - Congenital Deficiency of C2 and Factor B
AU - Raum, Donald
AU - Glass, David
AU - Agnello, Vincent
AU - Schur, Peter
AU - Alper, Chester A.
PY - 1978/12/7
Y1 - 1978/12/7
N2 - To the Editor: Recently, Newman et al.1 reported decreased levels of properdin factor B in three homozygous C2-deficient children, an association attributed to the linkage between genes coding for the two proteins. The authors cite the papers by Glass2 and Raum3 and their colleagues as in agreement. In the paper by Glass et al.2 the only person with homozygous C2 deficiency, a patient with systemic lupus erythematosus, had a factor B level of 320 μg per milliliter, which was within the normal range. This paper reported a statistical difference in factor B levels between heterozygous C2-deficient and normal family members.
AB - To the Editor: Recently, Newman et al.1 reported decreased levels of properdin factor B in three homozygous C2-deficient children, an association attributed to the linkage between genes coding for the two proteins. The authors cite the papers by Glass2 and Raum3 and their colleagues as in agreement. In the paper by Glass et al.2 the only person with homozygous C2 deficiency, a patient with systemic lupus erythematosus, had a factor B level of 320 μg per milliliter, which was within the normal range. This paper reported a statistical difference in factor B levels between heterozygous C2-deficient and normal family members.
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U2 - 10.1056/NEJM197812072992316
DO - 10.1056/NEJM197812072992316
M3 - Letter
C2 - 714103
AN - SCOPUS:0018262919
SN - 0028-4793
VL - 299
SP - 1313
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 23
ER -