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APA Citation
Leonhardt, A., Hauer, J., Ghiringhelli, N., Zhang, Y., Meyer, N., Goodfellow, R. X., Martin, B., Nester, C., & Smith, R. (n.d.). ultra-rare C3 mutation leading to a dominant familial C3 glomerulopathy phenotype. Molecular immunology, 89, 175–176. http://access.bl.uk/ark:/81055/vdc_100049903444.0x000031