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Volumn 18, Issue 1, 2003, Pages 3-18

Molecular diagnosis of unherited movement disorders. Movement disorders society task force on molecular diagnosis

Author keywords

Autosomal dominant cerebellar ataxias; Autosomal recessive ataxias; Essential tremor; Genetic testing; Huntington's disease; Parkinson's disease; Parkinsonism; Primary torsion dystonia; Wilson disease

Indexed keywords

ADENINE; ADENOSINE TRIPHOSPHATASE; ALPHA SYNUCLEIN; ALPHA TOCOPHEROL; APOLIPOPROTEIN B; ATM PROTEIN; CHOLESTANOL; COPPER; CYTOSINE; DNA; FRATAXIN; GENE PRODUCT; GUANINE; PHOSPHATIDYLINOSITOL 3 KINASE; PHYTANIC ACID; TYROSINE 3 MONOOXYGENASE;

EID: 0037249245     PISSN: 08853185     EISSN: None     Source Type: Journal    
DOI: 10.1002/mds.10338     Document Type: Review
Times cited : (35)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.