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S12881-015-0231-9
S12881-015-0231-9
http://dx.doi.org/10.1186/S12881-015-0231-9
NPHS2 mutations account for only 15% of nephrotic syndrome cases.
P356
Q35792721-7246EBF0-8DF3-4889-9989-B556A6B8C229
P356
S12881-015-0231-9
http://dx.doi.org/10.1186/S12881-015-0231-9