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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...
Autores principales: | Völker, Linus A, Schurek, Eva-Maria, Rinschen, Markus M, Tax, Judit, Schutte, Barbara A, Lamkemeyer, Tobias, Ungrue, Denise, Schermer, Bernhard, Benzing, Thomas, Höhne, Martin |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658879/ https://www.ncbi.nlm.nih.gov/pubmed/23648087 http://dx.doi.org/10.1186/1471-2369-14-102 |
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