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Q35792721-0335CDB1-6A6B-4E98-8567-682098D01F1B
Q35792721-0335CDB1-6A6B-4E98-8567-682098D01F1B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35792721-0335CDB1-6A6B-4E98-8567-682098D01F1B
NPHS2 mutations account for only 15% of nephrotic syndrome cases.
P2860
Q35792721-0335CDB1-6A6B-4E98-8567-682098D01F1B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35792721-0335CDB1-6A6B-4E98-8567-682098D01F1B
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wasDerivedFrom
23dfd63d901dc3d7f73eb09cbe3389ba35298396
P2860
Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS)