Analysis of IPSCs generated from LRRK2 (Gly2019Ser) mutation-bearing patient fibroblasts by cell reprogramming. The LRRK2 (G2019S) mutation causes familial Parkinson's disease (PD). Results provide insight into the molecular mechanisms underlying PD.
GPL571:
[HG-U133A_2] Affymetrix Human Genome U133A 2.0 Array
Citation:
Liu GH, Qu J, Suzuki K, Nivet E et al. Progressive degeneration of human neural stem cells caused by pathogenic LRRK2. Nature 2012 Nov 22;491(7425):603-7. PMID: 23075850