ID   PFIZi027-A
AC   CVCL_RG03
SY   B221c13
DR   BioSamples; SAMEA104243150
DR   EBiSC; PFIZi027-A
DR   ECACC; 66540612
DR   hPSCreg; PFIZi027-A
DR   Wikidata; Q54947281
CC   From: Pfizer, Inc.; New York; USA.
CC   Sequence variation: Mutation; HGNC; HGNC:2714; DCX; Unexplicit; Ex5-8del; Zygosity=Heterozygous (hPSCreg=PFIZi027-A).
CC   Discontinued: ECACC; 66540612; true.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C116573; Dravet syndrome
DI   ORDO; Orphanet_33069; Dravet syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   5-9Y
CA   Induced pluripotent stem cell
DT   Created: 05-03-18; Last updated: 19-12-24; Version: 10
//