ID   HPSI1016i-riwg_8
AC   CVCL_LM58
SY   WTSIi681-B; WTSIi712-A
DR   BioSamples; SAMEA104132682
DR   ECACC; 77650796
DR   HipSci; HPSI1016i-riwg_8
DR   hPSCreg; WTSIi681-B
DR   Wikidata; Q54891615
CC   From: Cambridge BioResource; Cambridge; United Kingdom.
CC   Population: Caucasian; Irish.
CC   Donor information: Donor is said to be suffering from a 'rare genetic neurological disorder'.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C26835; Nervous system disorder
DI   ORDO; Orphanet_71859; Rare genetic neurological disorder
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_LM57 ! HPSI1016i-riwg_2
SX   Female
AG   5-9Y
CA   Induced pluripotent stem cell
DT   Created: 15-11-17; Last updated: 29-06-23; Version: 10
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