Absence of mutation in the SLC2A1 gene in a cohort of patients with alternating hemiplegia of childhood (AHC)

Neuropediatrics

Volumn 41, Issue 6, 2010, Pages 267-269

  Vuillaumier Barrot, S ^a,b   Panagiotakaki, E ^c   Bizec, C Le ^a   Baba, C El ^d,e,f   Fontaine, B ^d,e,f,g   Arzimanoglou, A ^c,e   Seta, N ^a,h   Nicole, S ^d,e,f,g  

^a BICHAT HOSPITAL   (France)

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

^c HOSPICES CIVILS DE LYON   (France)

^d SORBONNE UNIVERSITÉ   (France)

^e INSERM   (France)

^f CNRS   (France)

^g PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^h UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

developmental neurology; epilepsy; genetics

Indexed keywords

GLUCOSE TRANSPORTER 1;

ADOLESCENT; ADULT; ALTERNATING HEMIPLEGIA OF CHILDHOOD; ARTICLE; CHILD; CHILDHOOD DISEASE; CLINICAL ARTICLE; COHORT ANALYSIS; FEMALE; GENE MUTATION; GENE SEQUENCE; HEMIPLEGIA; HUMAN; HUMAN CELL; MALE; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ADULT; AGE OF ONSET; ALLELES; CHILD; CHILD, PRESCHOOL; FEMALE; GENETIC ASSOCIATION STUDIES; GENOTYPE; GLUCOSE TRANSPORTER TYPE 1; HEMIPLEGIA; HUMANS; MALE; MIDDLE AGED; MUTATION;

EID: 79953250552     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0031-1271767     Document Type: Article

References (10)

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