SCOPUS 정보 검색 플랫폼

Volumn 68, Issue 6, 2001, Pages 1327-1332

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy

(6) Claes, Lieve a Del Favero, Jurgen a Ceulemans, Berten b,c Lagae, Lieven c,d Van Broeckhoven, Christine a De Jonghe, Peter a,b

a DEPARTMENT OF PLANT SYSTEMS BIOLOGY (Belgium)

b ANTWERP UNIVERSITY HOSPITAL (Belgium)

c Epilepsy Center for Children and Youth (Belgium)

d UNIVERSITY HOSPITALS LEUVEN (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PROTEIN SCN1A; SODIUM CHANNEL; SODIUM ION; UNCLASSIFIED DRUG;

ARTICLE; BELGIUM; CHANNEL GATING; CLINICAL ARTICLE; FEBRILE CONVULSION; FEMALE; FRAMESHIFT MUTATION; GENE MUTATION; HUMAN; HUMAN CELL; INFANT DISEASE; MALE; MISSENSE MUTATION; MYOCLONUS EPILEPSY; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; PRIORITY JOURNAL; PSYCHOMOTOR DEVELOPMENT; SCHOOL CHILD; SYMPTOMATOLOGY;

EID: 0034987073 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: 10.1086/320609 Document Type: Article

Times cited : (1093)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.