(Q83276005)
Statements
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 (English)
Yulia Grischuk
Marina Müller
Ruth Elisabeth Volk
Joachim Grötzinger
Paul-Martin Holterhus
Wolfgang G Sippell