ID   ND38262
AC   CVCL_EZ26
DR   Coriell; ND38262
DR   NHCDR; ND38262
DR   Wikidata; Q54930060
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Unspecified (NHCDR=ND38262).
CC   Discontinued: Coriell; ND38262; true.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
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   60Y
CA   Finite cell line
DT   Created: 26-09-16; Last updated: 19-12-24; Version: 12
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