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1. A rare S33C mutation of CTNNB1 encoding β-catenin in a parathyroid adenoma found in an Italian primary hyperparathyroid cohort.

Author

Guarnieri V, Baorda F, Battista C, Bisceglia M, Balsamo T, Gruppioni E, Fiorentino M, Muscarella LA, Coco M, Barbano R, Corbetta S, Spada A, Cole DE, Canaff L, Hendy GN, Carella M, and Scillitani A

Subjects
Adenoma epidemiology, Adenoma ethnology, Aged, Cohort Studies, Comorbidity, Exons genetics, Female, Humans, Hyperparathyroidism epidemiology, Hyperparathyroidism ethnology, Italy, Middle Aged, Parathyroid Neoplasms epidemiology, Parathyroid Neoplasms ethnology, Retrospective Studies, Adenoma genetics, Hyperparathyroidism genetics, Mutation genetics, Parathyroid Neoplasms genetics, beta Catenin genetics
Published
2012
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