Sign Up to like & get
recommendations!
0
Published in 2020 at "Frontiers in Endocrinology"
DOI: 10.3389/fendo.2020.591501
Abstract: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant inherited tumor syndrome, associated with parathyroid, pituitary, and gastro-entero-pancreatic (GEP) neuroendocrine tumors (NETs). MEN1 is usually consequent to different germline and somatic mutations of…
read more here.
Keywords:
associated men1;
genotype phenotype;
genotype;
men1 syndrome ... See more keywords