Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucocorticoid deficiency type 2

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Item Type:	Article
Title:	Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucocorticoid deficiency type 2
Creators Name:	Metherell, L.A., Cooray, S., Huebner, A., Rueschendorf, F., Naville, D., Begeot, M. and Clark, A.J.L.
Keywords:	Adenine, Glucocorticoids, Guanine, Homozygote, Inborn Errors Steroid Metabolism, Introns, Mutation, Pair 21 Human Chromosomes, Protein Transport, Thymine
Source:	Endocrine Research
ISSN:	0743-5800
Publisher:	Taylor & Francis
Volume:	30
Number:	4
Page Range:	889-890
Date:	1 January 2004
Official Publication:	https://doi.org/10.1081/ERC-200044136
PubMed:	View item in PubMed

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