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ASN.2013070732
ASN.2013070732
http://dx.doi.org/10.1681/ASN.2013070732
Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN.
P356
Q34427591-505E3B8E-6AF2-4836-B7A7-4F6F6290B143
P356
ASN.2013070732
http://dx.doi.org/10.1681/ASN.2013070732