ID   HPS0097
AC   CVCL_T964
DR   RCB; HPS0097
DR   SKIP; SKIP000617
DR   Wikidata; Q54890313
CC   Population: Japanese.
CC   Sequence variation: Mutation; HGNC; HGNC:8607; PRKN; Unexplicit; Not described; Zygosity=Unspecified (RCB=HPS0097).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C198603; Parkinson disease 2, autosomal recessive juvenile
DI   ORDO; Orphanet_2828; Young-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   50Y
CA   Induced pluripotent stem cell
DT   Created: 03-02-14; Last updated: 19-12-24; Version: 12
//