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Article

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

Endocrine research - 1 Nov 2004

Metherell Louise A, Cooray Sadani, Huebner Angela, Ruschendorf Franz, Naville Danielle, Begeot Martine, Clark Adrian J L

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PMID: 15666841
DOI: 10.1081/erc-200044136

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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