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Jessen, C.L., Christensen, J.H., Birkebaek, N.H. and Ritting, S. (2012) Homozygosity for a mutation in the CYP11B2 gene in an infant with congenital corticosterone methyl oxidase deficiency type II. Acta Paediatrica, 101, 519-525. http://dx.doi.org/10.1111/j.1651-2227.2012.02823.x

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