A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds

Journal of Clinical Endocrinology and Metabolism

Volumn 91, Issue 5, 2006, Pages 1943-1949

  Groussin, Lionel ^a,b   Horvath, Anelia ^c   Jullian, Eric ^a   Boikos, Sosipatros ^c   Rene Corail, Fernande ^a   Lefebvre, Herve ^d   Cephise Velayoudom, Fritz Line ^e   Vantyghem, Marie Christine ^e   Chanson, Philippe ^f   Conte Devolx, Bernard ^g   Lucas, Miguel ^h   Gentil, Alfonso ^h   Malchoff, Carl D ⁱ   Tissier, Frédérique ^a,b   Carney, J Aidan ^j   Bertagna, Xavier ^a,b   Stratakis, Constantine A ^c   Bertherat, Jérôme ^a,b,k  

^a INSERM   (France)

^b Hôpital Cochin ^*  (France)

^c EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

^d ROUEN UNIVERSITY HOSPITAL   (France)

^e LILLE UNIVERSITY HOSPITAL   (France)

^f Department of Endocrinology ^*  (France)

^g TIMONE HOSPITAL   (France)

^h HOSPITAL UNIVERSITARIO VIRGEN MACARENA   (Spain)

ⁱ UNIVERSITY OF CONNECTICUT HEALTH CENTER   (United States)

^j MAYO CLINIC   (United States)

^k Service d'Endocrinologie   (France)

more..

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA; PROTEIN KINASE; PROTEIN PRKAR1A; UNCLASSIFIED DRUG;

ADRENAL CORTEX INSUFFICIENCY; ADULT; ANAMNESIS; ARTICLE; CARNEY COMPLEX; CHROMOSOME 17; CLINICAL ARTICLE; CLINICAL FEATURE; CUSHING SYNDROME; EXON; FEMALE; GENE DELETION; GENE MUTATION; GENOTYPE; HEALTH CENTER; HUMAN; MALE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN ANALYSIS;

ADOLESCENT; ADRENAL CORTEX DISEASES; ADULT; CELLS, CULTURED; CUSHING SYNDROME; CYCLIC AMP-DEPENDENT PROTEIN KINASES; CYCLOHEXIMIDE; DNA; FEMALE; FOUNDER EFFECT; GENOTYPE; HAPLOTYPES; HUMANS; INTRONS; MALE; MUTATION; PEDIGREE; PENETRANCE; PHENOTYPE; PROTEIN SYNTHESIS INHIBITORS; RNA, MESSENGER;

NOTOLABRUS CELIDOTUS;

EID: 33646427720     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2005-2708     Document Type: Article

References (20)

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