ID   STBCi088-B
AC   CVCL_RD42
SY   SFC872-03-02
DR   BioSamples; SAMEA104493880
DR   EBiSC; STBCi088-B
DR   ECACC; 66540852
DR   hPSCreg; STBCi088-B
DR   Wikidata; Q54970195
CC   From: StemBANCC; Oxford; United Kingdom.
CC   Sequence variation: Mutation; HGNC; 4177; GBA1; Simple; p.Leu483Pro (c.1448T>C) (L444P); ClinVar=VCV000004288; Zygosity=Unspecified (EBiSC=STBCi088-B).
CC   Discontinued: ECACC; 66540852; true.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C26845; Parkinson's disease
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_RD41 ! STBCi088-A
OI   CVCL_RD43 ! STBCi088-C
SX   Male
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 30-01-24; Version: 13
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