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Volumn 67, Issue 9, 2006, Pages 1698-1700

POLG1 in idiopathic Parkinson disease

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; EXON; FEMALE; GENE; GENE FREQUENCY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; IDIOPATHIC DISEASE; ITALY; MAJOR CLINICAL STUDY; MALE; PARKINSON DISEASE; PARKINSONISM; POLG1 GENE; PRIORITY JOURNAL; UNITED KINGDOM;

EID: 33751008071     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000238963.07425.d5     Document Type: Article
Times cited : (43)

References (10)
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  • 3
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    • Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: Clinical and molecular genetic study
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  • 4
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    • A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and parkinsonism
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  • 5
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    • Chan, S.S.1    Longley, M.J.2    Copeland, W.C.3
  • 6
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    • (Amst)
    • Chan SS, Longley MJ, Naviaux RK, Copeland WC. Mono-allelic POLG expression resulting from nonsense-mediated decay and alternative splicing in a patient with Alpers syndrome. DNA Repair (Amst) 2005;4:1381-1389.
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  • 7
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.