Pub. Date : 2014 Oct
PMID : 25112471
2 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | NPHS2 variation in Chinese southern infants with late steroid-resistant nephrotic syndrome. | Steroids | NPHS2 stomatin family member, podocin | Homo sapiens |
| 2 | Abstract NPHS2 mutations are responsible for autosomal recessive familial steroid-resistant nephrotic syndrome (SRNS) with minor glomerular abnormalities or focal segmental glomerulosclerosis (FSGS), which is characterized by early childhood onset and rapid progression to chronic renal insufficiency. | Steroids | NPHS2 stomatin family member, podocin | Homo sapiens |