ID   PD-BP19-iPSC
AC   CVCL_JL86
DR   Wikidata; Q54946769
RX   PubMed=28395802;
CC   From: National Neuroscience Institute; Singapore; Singapore.
CC   Sequence variation: Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Arg1628Pro (c.4883G>C); ClinVar=VCV000039198; Zygosity=Heterozygous (PubMed=28395802).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
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   59Y
CA   Induced pluripotent stem cell
DT   Created: 15-05-17; Last updated: 19-12-24; Version: 11
//
RX   PubMed=28395802; DOI=10.1016/j.scr.2016.12.011;
RA   Ma D.-R., Zhou W., Ng E.Y.-L., Zeng L., Zhao Y., Tan E.K.;
RT   "Reprogramming of a human induced pluripotent stem cell (iPSC) line
RT   from a Parkinson's disease patient with a R1628P variant in the LRRK2
RT   gene.";
RL   Stem Cell Res. 18:45-47(2017).
//