ID   HPS3887
AC   CVCL_ZE14
SY   BRCi008-A
DR   hPSCreg; BRCi008-A
DR   SKIP; SKIP005798
DR   Wikidata; Q98126707
RX   PubMed=32413791;
CC   Population: Japanese.
CC   Sequence variation: Gene amplification; HGNC; 11138; SNCA; Duplication; Zygosity=Heterozygous (PubMed=32413791).
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C198604; Parkinson disease 4, autosomal dominant
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   52Y
CA   Induced pluripotent stem cell
DT   Created: 02-07-20; Last updated: 29-06-23; Version: 7
//
RX   PubMed=32413791; DOI=10.1016/j.scr.2020.101828;
RA   Suzuki H., Egawa N., Kondo T., Imamura K., Enami T., Tsukita K.,
RA   Suga M., Shibukawa R., Okanishi Y., Uchiyama T., Inoue H.,
RA   Takahashi R.;
RT   "Generation of a human induced pluripotent stem cell line derived from
RT   a Parkinson's disease patient carrying SNCA duplication.";
RL   Stem Cell Res. 45:101828-101828(2020).
//