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A novel variant in YWHAG further supports phenotype of developmental and epileptic encephalopathy.
Sedlácková, Lucie; Sterbová, Katalin; Vlcková, Markéta; Maulisová, Alice; Lassuthová, Petra.
Affiliation
  • Sedlácková L; Neurogenetic Laboratory, Department of Pediatric Neurology, Second Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic.
  • Sterbová K; Department of Pediatric Neurology, Second Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic.
  • Vlcková M; Biology and Medical Genetics, Second Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic.
  • Maulisová A; Department of Psychology, Second Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic.
  • Lassuthová P; Neurogenetic Laboratory, Department of Pediatric Neurology, Second Faculty of Medicine, Charles University in Prague and University Hospital Motol, Prague, Czech Republic.
Am J Med Genet A ; 185(5): 1363-1365, 2021 05.
Article in En | MEDLINE | ID: mdl-33590706
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Diseases / Mutation, Missense Limits: Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2021 Type: Article Affiliation country: Czech Republic
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Diseases / Mutation, Missense Limits: Humans Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2021 Type: Article Affiliation country: Czech Republic