Analyzing the functional and structural consequences of two point mutations (P94L and A368D) in the CYP11B1 gene causing congenital adrenal hyperplasia resulting from 11-hydroxylase deficiency

Nils Krone, Y Grischuk, M Muller, RE Volk, J Grotzinger, PM Holterhus, WG Sippell, FG Riepe

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