SCOPUS 정보 검색 플랫폼

Movement Disorders

Volumn 17, Issue 6, 2002, Pages 1390-1392

Hereditary chin trembling: A new family with exclusion of the chromosome 9q13-q21 locus

(5) Grimes, David A a,b Han, Fabin a Bulman, Dennise a Nicolson, Mary Lou c Suchowersky, Oksana c

a OTTAWA HOSPITAL RESEARCH INSTITUTE (Canada)

b Parkinsons Dis/Movt Disord Clin (Canada)

c UNIVERSITY OF CALGARY (Canada)

Author keywords

Chromosome 9q13 21; Herediatary chin trembling; Linkage analysis

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 9Q; CLINICAL ARTICLE; FAMILY STUDY; FEMALE; GENETIC LINKAGE; HEREDITARY CHIN TREMBLING; HUMAN; LINKAGE ANALYSIS; MALE; MOTOR DYSFUNCTION; PEDIGREE ANALYSIS; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AGED; BOTULINUM TOXIN TYPE A; CHIN; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; HUMANS; LINKAGE (GENETICS); MALE; MIDDLE AGED; PEDIGREE; TREMOR;

EID: 0036869117 PISSN: 08853185 EISSN: None Source Type: Journal
DOI: 10.1002/mds.10275 Document Type: Article

Times cited : (19)

References (8)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.