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HARVARD Citation
Leonhardt, A. et al. (n.d.). Ultra-rare C3 mutation leading to a dominant familial C3 glomerulopathy phenotype. Molecular immunology. pp. 175-176. [Online].
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Leonhardt, A. et al. (n.d.). Ultra-rare C3 mutation leading to a dominant familial C3 glomerulopathy phenotype. Molecular immunology. pp. 175-176. [Online].