Title : MEGDEL Syndrome - Finsterer_2020_Pediatr.Neurol_110_25 |
Author(s) : Finsterer J , Scorza FA , Fiorini AC , Scorza CA |
Ref : Pediatr Neurol , 110 :25 , 2020 |
Abstract : |
PubMedSearch : Finsterer_2020_Pediatr.Neurol_110_25 |
PubMedID: 32684373 |
Gene_locus related to this paper: human-SERAC1 |
Title : Dystonia is a Common Phenotypic Feature of MEGDEL Syndrome - Finsterer_2018_Tremor.Other.Hyperkinet.Mov.(N.Y)_8_568 |
Author(s) : Finsterer J , Scorza FA , Fiorini AC , Scorza CA , Almeida AC |
Ref : Tremor Other Hyperkinet Mov (N Y) , 8 :568 , 2018 |
Abstract : |
PubMedSearch : Finsterer_2018_Tremor.Other.Hyperkinet.Mov.(N.Y)_8_568 |
PubMedID: 29971201 |
Gene_locus related to this paper: human-SERAC1 |