ID   PI-1353-C7
AC   CVCL_RK99
SY   1353 C7
DR   Wikidata; Q54947374
RX   PubMed=22567022;
CC   Sequence variation: Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Unspecified (PubMed=22567022).
CC   Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C198605; Parkinson disease 8, autosomal dominant
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   55Y
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 19-12-24; Version: 10
//
RX   PubMed=22567022; DOI=10.1155/2012/140427; PMCID=PMC3339118;
RA   Mak S.K., Huang Y.A., Iranmanesh S., Vangipuram M., Sundararajan R.,
RA   Nguyen L., Langston J.W., Schule B.;
RT   "Small molecules greatly improve conversion of human-induced
RT   pluripotent stem cells to the neuronal lineage.";
RL   Stem Cells Int. 2012:140427.1-140427.12(2012).
//