The first confirmed case with C3 deficiency caused by compound heterozygous mutations in the C3 gene; a new aspect of pathogenesis for C3 deficiency

Autor: Kida, Miyuki a, Fujioka, Hirotaka b, Kosaka, Yoshiyuki c, Hayashi, Kouhei c, Sakiyama, Yukio d, Ariga, Tadashi a, ⁎
Zdroj: In Blood Cells, Molecules and Diseases 2008 40(3):410-413
Databáze: ScienceDirect