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
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| Description | scientific article published on 02 May 2006 |
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author: Nils Krone Paul-Martin Holterhus |
| Publication date | May 2, 2006 |
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