1 Ocak 2009 Dergi makalesi Açık Erişim

Pirkevi, C.; Lesage, S.; Condroyer, C.; Tomiyama, H.; Hattori, N.; Ertan, S.; Brice, A.; Basak, A. N.

JSON

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        "affiliation": "Bogazici Univ, Dept Mol Biol & Genet, Neurodegenerat Res Lab, TR-34342 Istanbul, Turkey", 
        "name": "Pirkevi, C."
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      {
        "name": "Lesage, S."
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      {
        "name": "Condroyer, C."
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      {
        "affiliation": "Juntendo Univ, Sch Med, Dept Neurol, Tokyo 113, Japan", 
        "name": "Tomiyama, H."
      }, 
      {
        "affiliation": "Juntendo Univ, Sch Med, Dept Neurol, Tokyo 113, Japan", 
        "name": "Hattori, N."
      }, 
      {
        "affiliation": "Univ Istanbul, Dept Neurol, Cerrahpasa Fac Med, TR-34098 Istanbul, Turkey", 
        "name": "Ertan, S."
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      {
        "name": "Brice, A."
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      {
        "affiliation": "Bogazici Univ, Dept Mol Biol & Genet, Neurodegenerat Res Lab, TR-34342 Istanbul, Turkey", 
        "name": "Basak, A. N."
      }
    ], 
    "description": "The leucine-rich repeat kinase 2 (LRRK2) G2019S mutation is recognized as the most common cause of familial autosomal dominant and also sporadic forms of Parkinson disease (PD). A common founder has been described for most Europeans and all North Africans and Jews; besides, two distinct G2019S LRRK2 haplotypes were found in a small proportion of European families and in Japanese PD patients. This study revealed a Turkish patient heterozygous for the G2019S mutation sharing the Japanese haplotype. To the best of our knowledge, it is the first time that the G2019S-associated Japanese haplotype has been reported in a different population.", 
    "doi": "10.1007/s10048-009-0173-5", 
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    "journal": {
      "issue": "3", 
      "pages": "271-273", 
      "title": "NEUROGENETICS", 
      "volume": "10"
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    "publication_date": "2009-01-01", 
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    "title": "A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype"
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