Novel Variations in KIRREL1 Gene and Infantile Onset Nephrotic Syndrome
Author:
Affiliation:
1. Division of Pediatric Nephrology, Department of Pediatrics, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India
Publisher
Scientific Scholar
Reference4 articles.
1. Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndrome;Solanki;Kidney Int,2019
2. NEPH1 defines a novel family of Podocin interacting proteins;Sellin;FASEB J,2003
3. Nephrin and neph1 co-localize at the podocyte foot process intercellular junction and form cis hetero-oligomers;Barletta;J Biol Chem,2003
4. Neph1, a component of the kidney slit diaphragm, is tyrosine-phosphorylated by the src family tyrosine kinase and modulates intracellular signaling by binding to grb2;Harita;J Biol Chem,2008
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