ID   NIMHi001-A
AC   CVCL_YT35
SY   BPPD01
DR   BioSamples; SAMEA6675820
DR   hPSCreg; NIMHi001-A
DR   SKIP; SKIP005731
DR   Wikidata; Q98127897
RX   PubMed=32244201;
CC   From: National Institute of Mental Health and Neurosciences; Bengaluru; India.
CC   Population: Indian.
CC   Sequence variation: Mutation; HGNC; 18618; LRRK2; Simple; p.Ile1371Val (c.4111A>G); ClinVar=VCV000039176; Zygosity=Heterozygous (PubMed=32244201).
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: 12-03-20; Last updated: 29-06-23; Version: 7
//
RX   PubMed=32244201; DOI=10.1016/j.scr.2020.101768;
RA   Datta I., Sowmithra X., Jagtap S., Potdar C., Yadav R., Pal P.K.;
RT   "Generation of induced pluripotent stem cells (NIMHi001-A) from a
RT   Parkinson's disease patient of East Indian ethnicity carrying LRRK2
RT   I1371V variant.";
RL   Stem Cell Res. 44:101768-101768(2020).
//