| scholarly article | Q13442814 |
| P50 | author | Charlie Tomson | Q51105169 |
| Matthew C Pickering | Q55692581 | ||
| P2093 | author name string | H Terence Cook | |
| Talat H Malik | |||
| Nicholas Medjeral-Thomas | |||
| Mitali P Patel | |||
| Tibor Toth | |||
| P2860 | cites work | Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis | Q24615589 |
| Dimerization of complement factor H-related proteins modulates complement activation in vivo | Q27676814 | ||
| Factor H family proteins: on complement, microbes and human diseases | Q33345389 | ||
| Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals. | Q33378236 | ||
| Location and structure of the human FHR-5 gene | Q34131162 | ||
| Genome-wide association study identifies susceptibility loci for IgA nephropathy | Q34170453 | ||
| Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigrees | Q35030648 | ||
| A hybrid CFHR3-1 gene causes familial C3 glomerulopathy. | Q36050943 | ||
| C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulation | Q36891110 | ||
| Recent insights into C3 glomerulopathy | Q38088187 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 933-937 | |
| P577 | publication date | 2013-09-25 | |
| P1433 | published in | Kidney International | Q6404823 |
| P1476 | title | A novel CFHR5 fusion protein causes C3 glomerulopathy in a family without Cypriot ancestry | |
| P478 | volume | 85 |
| Q37682273 | American Society of Nephrology clinical pathological conference |
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| Q35567846 | Pathogenesis of glomerular haematuria. |
| Q55385450 | Progressive IgA Nephropathy Is Associated With Low Circulating Mannan-Binding Lectin-Associated Serine Protease-3 (MASP-3) and Increased Glomerular Factor H-Related Protein-5 (FHR5) Deposition. |
| Q26741542 | Reclassification of membranoproliferative glomerulonephritis: Identification of a new GN: C3GN |
| Q58803464 | Reference Intervals of Factor H and Factor H-Related Proteins in Healthy Children |
| Q64044064 | Self-Damage Caused by Dysregulation of the Complement Alternative Pathway: Relevance of the Factor H Protein Family |
| Q37032691 | The Genetics of Ultra-Rare Renal Disease |
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| Q40744602 | Update on C3 glomerulopathy. |
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