Detection of somatic β-catenin mutations in primary pigmented nodular adrenocortical disease (PPNAD)

BACKGROUND: Primary pigmented nodular adrenocortical disease (PPNAD) leads to Cushing syndrome (CS) and is often associated with Carney complex (CNC). Genetic alterations of the type 1-α regulatory subunit of cAMP-dependent protein kinase A (PRKAR1A) and phosphodiesterase 11A4 (PDE11A) genes have be...

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Autores principales: Tadjine, Mimi, Lampron, Antoine, Ouadi, Lydia, Horvath, Anelia, Stratakis, Constantine A., Bourdeau, Isabelle
Formato: Artigo
Lenguaje:Inglês
Publicado: 2008
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3138207/
https://ncbi.nlm.nih.gov/pubmed/18419788
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2265.2008.03273.x
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