Novel X-linked glomerulopathy is associated with a COL4A5 missense mutation in a non-collagenous interruption.

Becknell B, Zender GA, Houston R, Baker PB, McBride KL, Luo W, Hains DS, Borza DB, Schwaderer AL
Kidney Int. 2011 79 (1): 120-7

PMID: 20881942 · PMCID: PMC3248803 · DOI:10.1038/ki.2010.354

MeSH Terms (13)

Adolescent Child Chromosomes, Human, X Collagen Type IV Female Glomerular Basement Membrane Glomerulonephritis Heterozygote Humans Kidney Failure, Chronic Male Mutation, Missense Pedigree

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