No evidence of ATP1A2 involvement in 12 multiplex Italian families with benign familial infantile seizures

Neuroscience Letters

Volumn 388, Issue 2, 2005, Pages 71-74

  Boneschi, Filippo Martinelli ^a   Aridon, Paolo ^a   Zara, Federico ^b   Guerrini, Renzo ^c   Marini, Carla ^c   De Fusco, Maurizio ^a   Comi, Giancarlo ^a   Casari, Giorgio ^a  

^a SAN RAFFAELE HOSPITAL   (Italy)

^b G GASLINI INSTITUTE   (Italy)

^c UNIVERSITY OF PISA   (Italy)

Author keywords

Benign familial infantile convulsions; Epilepsy; Familial hemiplegic migraine; Genetics

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); AMINO ACID; MESSENGER RNA;

ARTICLE; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; DNA SEQUENCE; EXON; FAMILIAL DISEASE; FAMILIAL HEMIPLEGIC MIGRAINE; FAMILY; GENE MUTATION; GENETIC CODE; GENETIC SCREENING; HUMAN; INTRON; MISSENSE MUTATION; PATHOGENESIS; PHYSIOLOGY; PRIORITY JOURNAL; SEIZURE;

EPILEPSY, BENIGN NEONATAL; EXONS; FAMILY HEALTH; HUMANS; INFANT; INTRONS; ITALY; MIGRAINE DISORDERS; MUTATION, MISSENSE; NA(+)-K(+)-EXCHANGING ATPASE;

EID: 23944497122     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2005.06.026     Document Type: Article

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