A Neonatal Form of Isolated ACTH Deficiency Frequently Associated with Tpit Gene Mutations
Authors: Jacques Drouin; M de Vroede; Raja Brauner; Wolfgang G. Sippell; Merih Berberoğlu; Jacques Weill; Thierry Brue; +23 Authors
Jacques Drouin; M de Vroede; Raja Brauner; Wolfgang G. Sippell; Merih Berberoğlu; Jacques Weill; Thierry Brue; Jennifer H. Kyllo; Sule Yigit; B. Pigeon; Michel David; F. de Zegher; Anne-Marie Pulichino; Anne Barlier; Leo Dunkel; Felix G. Riepe; Carl-Joachim Partsch; Cheri Deal; Georges Malpuech; K Noordam; Begüm Atasay; Sophie Vallette-Kasic; Patricia A. Donohoue; P Dechelotte; Juliane Léger; M. Gueydan; Martin Fassnacht; G. Van Vliet; Juan J. Heinrich; Alain Enjalbert;
pmid: 15666849
A Neonatal Form of Isolated ACTH Deficiency Frequently Associated with Tpit Gene Mutations
Related Organizations
- Montreal Clinical Research Institute Canada
- University of Montreal Canada
Keywords
Homeodomain Proteins, Steroid Metabolism, Inborn Errors, Adrenocorticotropic Hormone, Mutation, Infant, Newborn, Humans, Genes, Recessive, T-Box Domain Proteins, Transcription Factors
Homeodomain Proteins, Steroid Metabolism, Inborn Errors, Adrenocorticotropic Hormone, Mutation, Infant, Newborn, Humans, Genes, Recessive, T-Box Domain Proteins, Transcription Factors
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citations
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
popularity
Popularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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