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Volumn 123, Issue 10, 2000, Pages 2040-2045

A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16

Author keywords

Chromosome 16; Haplotypes; Linkage studies; Paroxysmal dyskinesia; Paroxysmal kinesigenic choreoathetosis

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHOREOATHETOSIS; CHROMOSOME 16Q; CHROMOSOME MAP; CONTROLLED STUDY; CONVULSION; DYSKINESIA; FEMALE; GENETIC LINKAGE; HAPLOTYPE; HUMAN; HUMAN CELL; INDIAN; MAJOR CLINICAL STUDY; MALE; MULTIGENE FAMILY; ONSET AGE; PRIORITY JOURNAL;

EID: 0033775093     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/123.10.2040     Document Type: Article
Times cited : (133)

References (25)
  • 4
    • 0001504349 scopus 로고
    • The paroxysmal dyskinesias
    • Marsden CD, Fahn S, editors. Movement disorders 3. Oxford: Butterworth-Heinmann
    • (1994) , pp. 310-345
    • Fahn, S.1
  • 11
    • 0014109480 scopus 로고
    • Paroxysmal kinesigenic choreoathetosis. An entity within the paroxysmal choreoathetosis syndrome. Description of 10 cases, including 1 autopsied
    • (1967) Neurology , vol.17 , pp. 680-690
    • Kertesz, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.