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Volumn 207, Issue 1-2, 2003, Pages 11-17

Pseudo-autosomal dominant inheritance of PARK2: Two families with parkin gene mutations

Author keywords

Exonic deletion; Gene dosage analysis; Haplotype; PARK2; Parkinson's disease; Pseudo dominant inheritance; The parkin gene

Indexed keywords

PARKIN;

EID: 12244283716     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-510X(02)00358-1     Document Type: Conference Paper
Times cited : (16)

References (9)
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    • Yamamura, Y.1    Kuzuhara, S.2    Kondo, K.3    Yanagi, T.4    Uchida, M.5    Matsumine, H.6
  • 3
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    • Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
    • Kitada T., Asakawa S., Hattori N., Matsumine H., Yamamura Y., Minoshima S.et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature. 392:1998;605-608.
    • (1998) Nature , vol.392 , pp. 605-608
    • Kitada, T.1    Asakawa, S.2    Hattori, N.3    Matsumine, H.4    Yamamura, Y.5    Minoshima, S.6
  • 5
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    • A microdeletion of D6S305 in a family of autosomal recessive juvenile parkinsonism (PARK2)
    • Matsumine H., Yamamura Y., Hattori N., Kobayashi T., Kitada T., Yoritaka A.et al. A microdeletion of D6S305 in a family of autosomal recessive juvenile parkinsonism (PARK2). Genomics. 49:1998;143-146.
    • (1998) Genomics , vol.49 , pp. 143-146
    • Matsumine, H.1    Yamamura, Y.2    Hattori, N.3    Kobayashi, T.4    Kitada, T.5    Yoritaka, A.6
  • 6
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    • Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization
    • Livak K.J., Flood S.J., Marmaro J., Giusti W., Deetz K. Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization. PCR Methods Appl. 4:1995;357-362.
    • (1995) PCR Methods Appl. , vol.4 , pp. 357-362
    • Livak, K.J.1    Flood, S.J.2    Marmaro, J.3    Giusti, W.4    Deetz, K.5
  • 8
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    • Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: Expanding the phenotype
    • Klein C., Pramstaller P.P., Kis B., Page C.C., Kann M., Leung J.et al. Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype. Ann. Neurol. 8:2000;65-71.
    • (2000) Ann. Neurol. , vol.8 , pp. 65-71
    • Klein, C.1    Pramstaller, P.P.2    Kis, B.3    Page, C.C.4    Kann, M.5    Leung, J.6
  • 9
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    • Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism
    • Maruyama M., Ikeuchi T., Saito M., Ishikawa A., Yuasa T., Tanaka H.et al. Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism. Ann. Neurol. 48:2000;245-250.
    • (2000) Ann. Neurol. , vol.48 , pp. 245-250
    • Maruyama, M.1    Ikeuchi, T.2    Saito, M.3    Ishikawa, A.4    Yuasa, T.5    Tanaka, H.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.