High prevalence of PROP1 gene mutations in Hungarian patients with childhood-onset combined anterior pituitary hormone deficiency

Endocrine

Volumn 30, Issue 3, 2006, Pages 255-260

  Halász, Zita ^a   Tőke, Judit ^b   Patócs, Attila ^b   Bertalan, Rita ^b   Tömböl, Zsófia ^b   Sallai, Ágnes ^a   Hosszú, Éva ^a   Muzsnai, Ágota ^c   Kovács, László ^d   Sólyom, János ^a   Fekete, György ^a   Rácz, Károly ^b  

^a SEMMELWEIS UNIVERSITY   (Hungary)

^b SEMMELWEIS UNIVERSITY OF MEDICINE   (Hungary)

^c Buda Children's Hospital   (Hungary)

^d NATIONAL MEDICAL CENTER   (Hungary)

Author keywords

Combined pituitary hormone deficiency; Hypopituitarism; Pituitary transcription factors; PROP1 gene

Indexed keywords

HYPOPHYSIS HORMONE; TRANSCRIPTION FACTOR PIT 1;

ADOLESCENT; ADULT; ARTICLE; CLINICAL ARTICLE; COMPARATIVE STUDY; CONTROLLED STUDY; EXON; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETICS; GROWTH HORMONE DEFICIENCY; GROWTH RETARDATION; HETEROZYGOSITY; HOMOZYGOSITY; HORMONE DEFICIENCY; HUMAN; HYPOPHYSIS; HYPOPLASIA; MALE; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; RADIOLOGY; SCHOOL CHILD;

EID: 34347360813     PISSN: 1355008X     EISSN: 15590100     Source Type: Journal    
DOI: 10.1007/s12020-006-0002-7     Document Type: Article

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