ID   PD-BP26-iPSC
AC   CVCL_JL87
DR   Wikidata; Q54946770
RX   PubMed=28395803;
CC   From: National Neuroscience Institute; Singapore; Singapore.
CC   Sequence variation: Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Arg1398His (c.4193G>A); ClinVar=VCV000039178; Zygosity=Heterozygous (PubMed=28395803).
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   Female
AG   72Y
CA   Induced pluripotent stem cell
DT   Created: 15-05-17; Last updated: 19-12-24; Version: 11
//
RX   PubMed=28395803; DOI=10.1016/j.scr.2016.12.014;
RA   Ma D.-R., Tio M., Ng S.H., Zeng L., Lim C.Y.-Y., Zhao Y., Tan E.K.;
RT   "Derivation of human induced pluripotent stem cell (iPSC) line with
RT   LRRK2 gene R1398H variant in Parkinson's disease.";
RL   Stem Cell Res. 18:48-50(2017).
//