← Evidence map

ArticleEndocrine2012

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

Vito Guarnieri et al.PubMed ↗Publisher ↗

No numbers read from the abstract.

10 papers cite it

2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 22095489