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00005392-200101000-00057
00005392-200101000-00057
http://dx.doi.org/10.1097/00005392-200101000-00057
Congenital anomalies of the kidney and urinary tract--role of the loss of function mutation in the pluripotent angiotensin type 2 receptor gene.
P356
Q34110254-C3526B17-9359-41FE-8BD5-BD28027EFA60
P356
00005392-200101000-00057
http://dx.doi.org/10.1097/00005392-200101000-00057