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2
NG.505
NG.505
http://dx.doi.org/10.1038/NG.505
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
P356
Q24292947-47D51FF2-A436-41E5-818A-6F4ECCC6D2EE
P356
NG.505
http://dx.doi.org/10.1038/NG.505