reference/5170406

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/5170406

Outgoing Links

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endingPage	1632
issn	0026-0495
issueIdentifier	11
pageRange	1628-1632
publicationName	Metabolism: clinical and experimental
startingPage	1628
bibliographicCitation	Katsumata N, Shinagawa T, Horikawa R, Fujikura K. Novel intronic CYP21A2 mutation in a Japanese patient with classic salt-wasting steroid 21-hydroxylase deficiency. Metabolism. 2010 Nov;59(11):1628–32. doi: 10.1016/j.metabol.2010.03.012. PMID: 20423741.
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date	201011
identifier	https://doi.org/10.1016/j.metabol.2010.03.012 https://pubmed.ncbi.nlm.nih.gov/20423741
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Novel intronic CYP21A2 mutation in a Japanese patient with classic salt-wasting steroid 21-hydroxylase deficiency
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Total number of triples: 48.