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Volumn 60, Issue 12, 2003, Pages 1961-1967

Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy

(27)  Nabbout, Rima a,b,c   Gennaro, E b   Dalla Bernardina, B d   Dulac, O c,e   Madia, F c   Bertini, E f   Capovilla, G g   Chiron, C c   Cristofori, G h   Elia, M i   Fontana, E d   Gaggero, R j   Granata, T k   Guerrini, R l,m   Loi, M n   La Selva, L o   Lispi, M L f   Matricardi, A b   Romeo, A p   Tzolas, V q   more..

e INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BENIGN CHILDHOOD EPILEPSY; CHILD; DISEASE SEVERITY; FAMILY HISTORY; FEMALE; GENE; GENE MUTATION; GENETIC HETEROGENEITY; GENOTYPE PHENOTYPE CORRELATION; HEREDITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; MYOCLONUS EPILEPSY; PRIORITY JOURNAL; SCN1A GENE; SEIZURE;

EID: 10744226685     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000069463.41870.2F     Document Type: Article
Times cited : (239)

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