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GFQ088
GFQ088
http://dx.doi.org/10.1093/NDT/GFQ088
Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS)
P356
Q34169609-423F2A45-44A1-4DDA-88A7-C0ED5C54954A
P356
GFQ088
http://dx.doi.org/10.1093/NDT/GFQ088