Steroid 11-beta hydroxylase deficiency caused by compound heterozygosity for a novel mutation in intron 7 (IVS 7 DS+4A to G) in one CYP11B1 allele and R448H in exon 8 in the other
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| Description | scientific article published on 22 December 2009 |
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author: Katarina Stingl |
| Publication date | December 22, 2009 |
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