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, ⁎ |
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Zdroj: | In Blood Cells, Molecules and Diseases 2008 40(3):410-413 |
Databáze: | ScienceDirect |
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