1 Ocak 2009 Dergi makalesi Açık Erişim

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

Citation Style Language JSON

{
  "DOI": "10.1007/s10048-009-0173-5", 
  "abstract": "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.", 
  "author": [
    {
      "family": "Pirkevi", 
      "given": " C."
    }, 
    {
      "family": "Lesage", 
      "given": " S."
    }, 
    {
      "family": "Condroyer", 
      "given": " C."
    }, 
    {
      "family": "Tomiyama", 
      "given": " H."
    }, 
    {
      "family": "Hattori", 
      "given": " N."
    }, 
    {
      "family": "Ertan", 
      "given": " S."
    }, 
    {
      "family": "Brice", 
      "given": " A."
    }, 
    {
      "family": "Basak", 
      "given": " A. N."
    }
  ], 
  "container_title": "NEUROGENETICS", 
  "id": "40951", 
  "issue": "3", 
  "issued": {
    "date-parts": [
      [
        2009, 
        1, 
        1
      ]
    ]
  }, 
  "page": "271-273", 
  "title": "A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype", 
  "type": "article-journal", 
  "volume": "10"
}