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Type and frequency of mutations in the LRRK2 gene in familial ans sporadic Parkinson's disease.

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اقرأ أكثر حفظ في قائمتي
  • معلومة اضافية
    • بيانات النشر:
      Oxford Univ. Press
    • الموضوع:
      2005
    • Collection:
      PuSH - Publikationsserver des Helmholtz Zentrums München
    • File Description:
      application/pdf
    • ISSN:
      0006-8950
      1460-2156
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/16251215; info:eu-repo/semantics/altIdentifier/wos/undefined; info:eu-repo/semantics/altIdentifier/isbn/0006-8950; info:eu-repo/semantics/altIdentifier/pissn/0006-8950; info:eu-repo/semantics/altIdentifier/eissn/1460; https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=3522; urn:isbn:0006-8950; urn:issn:0006-8950; urn:issn:1460-2156
    • الدخول الالكتروني :
      https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=3522
    • Rights:
      info:eu-repo/semantics/openAccess
    • الرقم المعرف:
      edsbas.BE5648E2