Parkinson’s Disease line with LRRK2 mutation. Additional clones from this iPS cell line (SUSL-046_C1 and SUSL-046_C2) are available from WiCell.

  • Unit of Measure (UOM) vial
  • Cell Type Human iPS
  • Sex Male
  • Age at Collection 65 years
  • Reprogramming Method Non-Integrating (Episomal Plasmid: Oct4, Klf4, Sox2, L-Myc)
  • Tissue Origin Skin Fibroblast
  • Genetic Alteration Mutation Information LRRK2, p.G2019S Homozygous
  • Disease Parkinson's Disease
  • Ethnicity Caucasian
  • Genetic Alteration Mutation LRRK2
  • hPSCReg ID MJFFi001-C
  • Provider The Michael J. Fox Foundation for Parkinson’s Research
  • Collections
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