Characterization of a short isoform of the kidney protein podocin in human kidney

BACKGROUND: Steroid resistant nephrotic syndrome is a severe hereditary disease often caused by mutations in the NPHS2 gene. This gene encodes the lipid binding protein podocin which localizes to the slit diaphragm of podocytes and is essential for the maintenance of an intact glomerular filtration...

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Main Authors: Völker, Linus A, Schurek, Eva-Maria, Rinschen, Markus M, Tax, Judit, Schutte, Barbara A, Lamkemeyer, Tobias, Ungrue, Denise, Schermer, Bernhard, Benzing, Thomas, Höhne, Martin
Formáid: Artigo
Teanga:Inglês
Foilsithe: BioMed Central 2013
Ábhair:
Research Article
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3658879/
https://ncbi.nlm.nih.gov/pubmed/23648087
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2369-14-102
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