Nonclassic steroid 21-hydroxylase deficiency due to a homozygous V281L mutation in CYP21A2 detected by the neonatal mass-screening program in Japan
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| Description | scientific article published on 30 November 2007 |
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author: Tsuyoshi Isojima Reiko Horikawa |
| Publication date | November 30, 2007 |
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