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DC08-1188
DC08-1188
http://dx.doi.org/10.2337/DC08-1188
Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes
P356
Q37022929-E0165113-E47B-4904-9AAD-08451562E55D
P356
DC08-1188
http://dx.doi.org/10.2337/DC08-1188