ID   WAe009-A-1C
AC   CVCL_D1GC
SY   ZZUSAe010-A-1C
DR   BioSamples; SAMEA114466775
DR   hPSCreg; WAe009-A-1C
DR   Wikidata; Q127384683
RX   PubMed=38428348;
CC   From: Zhengzhou University Second Affiliated Hospital; Zhengzhou; China.
CC   Sequence variation: Mutation; HGNC; HGNC:2928; DMD; Simple_edited; c.7285+2T>C; Zygosity=Homozygous; Note=By CRISPR/Cas9. Splice donor mutation (PubMed=38428348).
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
DI   NCIt; C75482; Duchenne muscular dystrophy
DI   ORDO; Orphanet_98896; Duchenne muscular dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_9773 ! WA09
SX   Female
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 30-01-24; Last updated: 19-12-24; Version: 3
//
RX   PubMed=38428348; DOI=10.1016/j.scr.2024.103343;
RA   Jin H., Fu H., Wang J.-J., Wang Z.-M., Liu J., Han F.-J., Zheng H.-J.,
RA   Jiang Y.-X.;
RT   "Generation of a DMD loss-of-function mutant human embryonic stem cell
RT   lines by CRISPR base editing.";
RL   Stem Cell Res. 76:103343-103343(2024).
//