Sequeira_2017_Neuropediatrics_48_382

Reference

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

Related information

Gene_locus related to this paper: human-SERAC1

Citations formats

Sequeira S, Rodrigues M, Jacinto S, Wevers RA, Wortmann SB (2017)
MEGDEL Syndrome: Expanding the Phenotype and New Mutations
Neuropediatrics 48 :382

Sequeira S, Rodrigues M, Jacinto S, Wevers RA, Wortmann SB (2017)
Neuropediatrics 48 :382