A novel in-frame deletion in MEN1 (p.Ala416del) causes familial multiple endocrine neoplasia type 1 with an aggressive phenotype and unexpected inheritance pattern.
Molecular medicine reports | 2016-09-01 | PMID 27430871
Skalniak Anna, Sokołowski Grzegorz, Jabrocka-Hybel Agata and 5 more
Genes: MEN1
