Next-generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson’s syndrome

The study of mutations causing the steroid-resistant nephrotic syndrome in children has greatly advanced our understanding of the kidney filtration barrier. In particular, these genetic variants have illuminated the roles of the podocyte, glomerular basement membrane and endothelial cell in glomerul...

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Detalhes bibliográficos
Publicado no:J Pathol
Main Authors: Bull, Katherine R, Mason, Thomas, Rimmer, Andrew J, Crockford, Tanya L, Silver, Karlee L, Bouriez-Jones, Tiphaine, Hough, Tertius A, Chaudhry, Shirine, Roberts, Ian SD, Goodnow, Christopher C, Cornall, Richard J
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Ltd 2013
Assuntos:
Original Papers
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4241031/
https://ncbi.nlm.nih.gov/pubmed/24293254
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/path.4308
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