No mutation in the SLC2A3 gene in cohorts of GLUT1 deficiency syndrome–like patients negative for SLC2A1 and in patients with AHC negative for ATP1A3

JIMD Reports

Volumn 12, Issue , 2014, Pages 115-120

  Bizec, C Le ^a   Nicole, S ^b,c,d   Panagiotakaki, E ^e   Seta, N ^a,f   Vuillaumier Barrot, S ^a,g  

^a BICHAT HOSPITAL   (France)

^b INSTITUT DU CERVEAU ET DE LA MOELLE ÉPINIÈRE   (France)

^c INSERM   (France)

^d CNRS   (France)

^e HOSPICES CIVILS DE LYON   (France)

^f UNIVERSITÉ PARIS DESCARTES   (France)

^g CENTRE DE RECHERCHE BIOMÉDICALE BICHAT BEAUJON CRB3   (France)

Author keywords

Dominant mutation; Heterozygous snps; Paroxysmal dyskinesia; SLC2A1 Gene; SLC2A1 Mutation

Indexed keywords

EID: 85028494674     PISSN: 21928304     EISSN: 21928312     Source Type: Book Series    
DOI: 10.1007/8904_2013_253     Document Type: Chapter

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