Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD)

Clinical Endocrinology

Volumn 70, Issue 1, 2009, Pages 96-103

  Kelberman, D ^a   Turton, J P G ^a   Woods, K S ^a   Mehta, A ^a   Al Khawari, M ^b   Greening, J ^c   Swift, P G F ^c   Otonkoski, T ^d   Rhodes, S J ^e   Dattani, M T ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b AL AMIRI HOSPITAL   (Kuwait)

^c LEICESTER ROYAL INFIRMARY   (United Kingdom)

^d UNIVERSITY OF HELSINKI   (Finland)

^e INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR PROP1; UNCLASSIFIED DRUG;

ADOLESCENT; ARTICLE; CHILD; CLINICAL ARTICLE; CONSANGUINEOUS MARRIAGE; CONTROLLED STUDY; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENE LOCUS; GENETIC ANALYSIS; HETEROZYGOSITY; HOMOZYGOSITY; HORMONE DEFICIENCY; HUMAN; INFANT; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; PEDIGREE ANALYSIS; PHENOTYPE; PITUITARY HORMONE DEFICIENCY; POINT MUTATION; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; TRANSCRIPTION INITIATION;

ADOLESCENT; ANIMALS; CHILD; CHILD, PRESCHOOL; CHO CELLS; COHORT STUDIES; CRICETINAE; CRICETULUS; DNA MUTATIONAL ANALYSIS; FEMALE; GENE DELETION; HOMEODOMAIN PROTEINS; HUMANS; HYPOPITUITARISM; INFANT; MALE; PEDIGREE; PITUITARY HORMONES;

EID: 58149156124     PISSN: 03000664     EISSN: 13652265     Source Type: Journal    
DOI: 10.1111/j.1365-2265.2008.03326.x     Document Type: Article

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