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

Endocrine Research

Volumn 30, Issue 4, 2004, Pages 943-944

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

^a CLIN RESEARCH INSTITUTE OF MONTREAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

T BOX TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR TPIT; UNCLASSIFIED DRUG;

CLINICAL ARTICLE; CONFERENCE PAPER; CONTROLLED STUDY; CORTICOTROPIN DEFICIENCY; DISEASE TRANSMISSION; EXON; GENE MUTATION; HETEROZYGOTE; HOMOZYGOTE; HORMONE SUBSTITUTION; HUMAN; NEWBORN DEATH; PHENOTYPE; PRIORITY JOURNAL;

ADRENOCORTICOTROPIC HORMONE; GENES, RECESSIVE; HOMEODOMAIN PROTEINS; HUMANS; INFANT, NEWBORN; MUTATION; STEROID METABOLISM, INBORN ERRORS; TRANSCRIPTION FACTORS;

EID: 19944428665     PISSN: 07435800     EISSN: None     Source Type: Journal    
DOI: 10.1081/ERC-200044166     Document Type: Conference Paper

References (0)