[HTML] sciencedirect.com

[HTML][HTML] Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion gene

X Xiao, C Ghossein, A Tortajada, Y Zhang, N Meyer… - Molecular …, 2016 - Elsevier
Abstract C3 glomerulopathy (C3G) is an ultra-rare complement-mediated renal disease
characterized histologically by the predominance of C3 deposition within in the glomerulus …
被引用次数：55 相关文章

Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion gene.

X Xiao, C Ghossein, A Tortajada, Y Zhang… - Molecular …, 2016 - europepmc.org
C3 glomerulopathy (C3G) is an ultra-rare complement-mediated renal disease
characterized histologically by the predominance of C3 deposition within in the glomerulus …

[引用][C] Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion gene

X Xiao, C Ghossein, A Tortajadam… - Molecular …, 2016 - produccioncientifica.ucm.es

Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion gene

X Xiao, C Ghossein, A Tortajada… - Molecular …, 2016 - pubmed.ncbi.nlm.nih.gov
C3 glomerulopathy (C3G) is an ultra-rare complement-mediated renal disease
characterized histologically by the predominance of C3 deposition within in the glomerulus …

Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion gene

X Xiao, C Ghossein, A Tortajada, Y Zhang… - Molecular …, 2016 - iro.uiowa.edu
A novel CFHR5–CFHR2 fusion gene was identified as a cause of familial C3GN.• The fusion
gene segregates with disease and is translated to a novel serum protein comprised of a …

Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion gene

X Xiao, C Ghossein, A Tortajada, Y Zhang… - Molecular …, 2016 - infona.pl
C3 glomerulopathy (C3G) is an ultra-rare complement-mediated renal disease
characterized histologically by the predominance of C3 deposition within in the glomerulus …

[引用][C] Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion gene

X Xiao, C Ghossein, A Tortajada, Y Zhang… - Molecular …, 2016 - cir.nii.ac.jp

Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion gene

X Xiao, C Ghossein, A Tortajadam… - Molecular …, 2016 - scholars.northwestern.edu
Abstract C3 glomerulopathy (C3G) is an ultra-rare complement-mediated renal disease
characterized histologically by the predominance of C3 deposition within in the glomerulus …

[引用][C] Familial C3 glomerulonephritis caused by a novel CFHR5-CFHR2 fusion gene

X Xiao, C Ghossein, A Tortajada, Y Zhang, N Meyer… - 2016