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Article

A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutations.

Endocrine research - 1 Nov 2004

Vallette-Kasic S, Pulichino A M, Gueydan M, Barlier A, David M, Malpuech G, Deal C, Van Vliet G, de Vroede M, Riepe F, Partsch C J, Sippell W, Berberoglu M, Atasay B, de Zegher F, Kyllo J, Donohoue P, Dechelotte P, Fassnacht M, Noordam K, Dunkel L, Pigeon B, Weill J, Yigit S, Brauner R, Leger J, Heinrich J J, Enjalbert A, Brue T, Drouin J

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Share to Adrenocorticotropic Hormone
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15666849
DOI: 10.1081/erc-200044166

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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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A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutations.PMID 15666849Read ↗

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