Title : MEGDEL Syndrome: Expanding the Phenotype and New Mutations - |
Author(s) : Sequeira S , Rodrigues M , Jacinto S , Wevers RA , Wortmann SB |
Ref : Neuropediatrics , 48 :382 , 2017 |
PubMedID: 28505671 |
Gene_locus related to this paper: human-SERAC1 |