Scorza CA

References (2)

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