ID   ZSYYDNi001-A
AC   CVCL_B5GP
SY   ZSYYDN-DMD-001
DR   hPSCreg; ZSYYDNi001-A
DR   Wikidata; Q110434444
RX   PubMed=34619646;
CC   From: Department of Neurology, Sun Yat-sen University First Affiliated Hospital; Guangzhou; China.
CC   Population: Chinese; Han.
CC   Sequence variation: Mutation; HGNC; HGNC:2928; DMD; Unexplicit; Ex51del; Zygosity=Hemizygous (PubMed=34619646).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C75482; Duchenne muscular dystrophy
DI   ORDO; Orphanet_98896; Duchenne muscular dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   8Y
CA   Induced pluripotent stem cell
DT   Created: 16-12-21; Last updated: 19-12-24; Version: 5
//
RX   PubMed=34619646; DOI=10.1016/j.scr.2021.102553;
RA   Wang L., Li H., Li Y.-Q., Xu M., Lin J.-F., Liao Z.-Y., Pei Z.,
RA   Zhang C.;
RT   "Generation and characterization of an induced pluripotent stem cell
RT   line (ZSYYDNi001-A) from a patient with Duchenne muscular dystrophy
RT   carrying exon 51 deletion in the DMD gene.";
RL   Stem Cell Res. 56:102553-102553(2021).
//