Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson's disease

• Naomi Seki

• Yuji Takahashi

• Hiroyuki Tomiyama

Bibliographic Information

Other Title

• Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson s disease

Journal

• Journal of human genetics / Japan Society of Human Genetics

  Journal of human genetics / Japan Society of Human Genetics 56 (9), 671-675, 2011-09

  Tokyo : Springer Nature

Keywords

• comprehensive mutational analysis
• LRRK2
• microarray-based resequencing
• Parkinson's disease
• p.G2385R

Details

• CRID: 1523388079992702592
• NII Article ID: 10030660937
• NII Book ID: AA11206160
• ISSN: 14345161
• NDL BIB ID: 11245408
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I11245408
• Web Site: https://search.jamas.or.jp/link/ui/2012139093
• Text Lang: en
• NDL Source Classification:
  • ZS16(科学技術--医学--人類遺伝学)
• Data Source:
  • NDL
  • CiNii Articles