ID   UKKi016-A
AC   CVCL_VF33
SY   NP0078-10
DR   BioSamples; SAMEA104615854
DR   EBiSC; UKKi016-A
DR   ECACC; 66540886
DR   hPSCreg; UKKi016-A
DR   Wikidata; Q54990430
CC   From: Institute for Neurophysiology, Medical Faculty; University of Cologne; Germany.
CC   Sequence variation: Heterozygous for KCNQ1 p.Arg366Trp (c.1096 C>T) (EBiSC).
DI   NCIt; C85049; Long QT syndrome 1
DI   ORDO; Orphanet_101016; Romano-Ward syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens
OI   CVCL_VF34 ! UKKi016-B
OI   CVCL_VF35 ! UKKi016-C
SX   Male
AG   30-34Y
CA   Induced pluripotent stem cell
DT   Created: 14-05-18; Last updated: 12-03-20; Version: 4
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