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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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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2008
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| Matèries: | |
| Accés en línia: | 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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