Title : [A genetic viewpoint of focal glomerular sclerosis: fom genes to glomerular pathophysiology [corrected]].

Pub. Date : 2003 Jul-Aug

PMID : 14523896






1 Functional Relationships(s)
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1 Because the majority of FSGS cases occur as sporadic disease, the recently described mutations in the NPHS2 gene "in approximately 25 percent of cases of apparently sporadic, steroid-resistant FSGS in children" have claimed great interest. Steroids NPHS2 stomatin family member, podocin Homo sapiens