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Volumn 9, Issue 5, 2003, Pages 313-314

Sensory neuropathy in autosomal recessive juvenile parkinsonism (PARK2)

Author keywords

Autosomal recessive juvenile parkinsonism; PARK2; Parkin; Parkinson's disease; Peripheral neuropathy; Sensory neuropathy

Indexed keywords

BROMOCRIPTINE; LEVODOPA; PARKIN; TRIHEXYPHENIDYL;

EID: 0038022575     PISSN: 13538020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1353-8020(02)00114-1     Document Type: Article
Times cited : (25)

References (8)
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    • Clinical analysis of 17 patients in 12 Japanese families with autosomal recessive type juvenile parkinsonism
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  • 5
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    • Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
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  • 6
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    • Molecular genetic analysis of a novel parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the parkin gene in affected individuals
    • Hattori N., Kitada T., Matsumine H., Asakawa S., Yamamura Y., Yoshino H., et al. Molecular genetic analysis of a novel parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the parkin gene in affected individuals. Ann Neurol. 44:1998;935-941.
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    • Familial parkinson's disease gene product, Parkin, is a ubiquitin-protein ligase
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.