PubMed:29049388 / 0-224 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/29049388","sourcedb":"PubMed","sourceid":"29049388","source_url":"https://www.ncbi.nlm.nih.gov/pubmed/29049388","text":"An inducible mouse model of podocin-mutation-related nephrotic syndrome.\nMutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early 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