Recurrent hemolytic-uremic syndrome with the hypomorphic fast allele of the third component of complement
- 31 October 1985
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 107 (4) , 564-566
- https://doi.org/10.1016/s0022-3476(85)80022-6
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Hypomorphic variant of the slow allele of C3 associated with hypocomplementemia and hematuriaThe American Journal of Medicine, 1985
- Genetically determined variation in the complement system: Relationship to diseaseThe Journal of Pediatrics, 1984
- An inherited defect in the C3 convertase, C3b,Bb, associated with glomerulonephritisKidney International, 1983
- Familial partial deficiency of the third component of complement (C3) and the hypocomplementemic cutaneous vasculitis syndromeThe American Journal of Medicine, 1980
- Partial Lipodystrophy and Familial C3 DeficiencyHuman Heredity, 1980
- Hypomorphic variant of C3, arthritis, and chronic glomerulonephritisThe Journal of Pediatrics, 1978
- Studies of a hypomorphic variant of human C3Journal of Clinical Investigation, 1971