reference/31539304

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endingPage	1025
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pageRange	1021-1025
publicationName	Endocrine Journal
startingPage	1021
bibliographicCitation	Shinagawa T, Horikawa R, Isojima T, Naiki Y, Tanaka T, Katsumata N. Nonclassic steroid 21-hydroxylase deficiency due to a homozygous V281L mutation in CYP21A2 detected by the neonatal mass-screening program in Japan. Endocr J. 2007 Dec;54(6):1021–5. doi: 10.1507/endocrj.k07-028. PMID: 18048990.
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date	200712
identifier	https://doi.org/10.1507/endocrj.k07-028 https://pubmed.ncbi.nlm.nih.gov/18048990
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	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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