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相模原常染色体優性パーキンソニズムにおける原因遺伝子の同定と発症機構の解析

相模原常染色体優性パーキンソニズムにおける原因遺伝子の同定と発症機構の解析
Paper図書
長谷川一子, 国立病院機構相模原病院臨床研究センター [著][長谷川一子]2004-2005<Y151-H16590843>
National Diet Library
  • Subject HeadingPARK8 / LRRK2/DRDN / I2020T / famil...

Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries

Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries
Digital博士論文
Tomiyama, HiroyukiWiley InterScience2006-04-18Movement Disorders21 8p.1102-1108
Available onlineOther Libraries in Japan
  • Subject Headinggenetics Parkinson’s disease PARK8 leucin rich repeat kinase 2 (...

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