Familial C3 Glomerulopathy Associated withCFHR5Mutations: Clinical Characteristics of 91 Patients in 16 Pedigrees-Reference-Cited by-同舟云学术

Familial C3 Glomerulopathy Associated withCFHR5Mutations: Clinical Characteristics of 91 Patients in 16 Pedigrees

Published:2011-05-12 Issue:6 Volume:6 Page:1436-1446
ISSN:1555-9041
Container-title:Clinical Journal of the American Society of Nephrology
language:en
Short-container-title:CJASN

Author:

Athanasiou Yiannis,Voskarides Konstantinos,Gale Daniel P.,Damianou Loukas,Patsias Charalambos,Zavros Michalis,Maxwell Patrick H.,Cook H. Terence,Demosthenous Panayiota,Hadjisavvas Andreas,Kyriacou Kyriacos,Zouvani Ioanna,Pierides Alkis,Deltas Constantinos

Publisher

American Society of Nephrology (ASN)

Subject

Transplantation,Nephrology,Critical Care and Intensive Care Medicine,Epidemiology

Reference33 articles.

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4. X-Linked Alport Syndrome: Natural History and Genotype-Phenotype Correlations in Girls and Women Belonging to 195 Families: A “European Community Alport Syndrome Concerted Action” Study

5. Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidney disease from focal segmental glomerulosclerosis

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