Associated Papers
Whole-exome sequencing as a tool for searching for genetic background modifiers in MEN1 patients with neuroendocrine pancreatic tumours, including insulinomas.
Skalniak A et al.
Endokrynologia Polska, 2023
Phenotypes Associated With MEN1 Syndrome: A Focus on Genotype-Phenotype Correlations.
Mele C et al.
Frontiers in Endocrinology, 2020
A novel in-frame deletion in MEN1 (p.Ala416del) causes familial multiple endocrine neoplasia type 1 with an aggressive phenotype and unexpected inheritance pattern.
Skalniak A et al.
Molecular Medicine Reports, 2016
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