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SREP39121
SREP39121
http://dx.doi.org/10.1038/SREP39121
The prevalence of CTNNB1 mutations in primary aldosteronism and consequences for clinical outcomes.
P356
Q37593326-F212E85E-641E-463A-AE21-4A7BC17C61C3
P356
SREP39121
http://dx.doi.org/10.1038/SREP39121