A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutations. Endocr Res 2004 Nov;30(4):943-4
Date
01/26/2005Pubmed ID
15666849DOI
10.1081/erc-200044166Scopus ID
2-s2.0-19944428665 (requires institutional sign-in at Scopus site) 8 CitationsAuthor List
Vallette-Kasic S, Pulichino AM, Gueydan M, Barlier A, David M, Malpuech G, Deal C, Van Vliet G, de Vroede M, Riepe F, Partsch CJ, 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 JJ, Enjalbert A, Brue T, Drouin JMESH terms used to index this publication - Major topics in bold
Adrenocorticotropic HormoneGenes, Recessive
Homeodomain Proteins
Humans
Infant, Newborn
Mutation
Steroid Metabolism, Inborn Errors
T-Box Domain Proteins
Transcription Factors
