ID   XMDYYYi001-A
AC   CVCL_A1ZV
SY   BDU-iPSCs
DR   BioSamples; SAMEA7683945
DR   hPSCreg; XMDYYYi001-A
DR   Wikidata; Q105511782
RX   PubMed=33799273;
CC   From: Department of Neurology, The First Affiliated Hospital of Xiamen University; Xiamen; China.
CC   Population: Asian.
CC   Sequence variation: Mutation; HGNC; 2928; DMD; Unexplicit; Ex2-19dup; Zygosity=Hemizygous (PubMed=33799273).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C84587; Becker's muscular dystrophy
DI   ORDO; Orphanet_98895; Becker muscular dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   44Y
CA   Induced pluripotent stem cell
DT   Created: 12-01-21; Last updated: 29-06-23; Version: 4
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RX   PubMed=33799273; DOI=10.1016/j.scr.2021.102298;
RA   Wang D., Lin J.-J., Jin M., Wang N.;
RT   "Establishment of a human iPSC line XMDYYYi001-A from a patient with
RT   Becker muscular dystrophy harboring duplications of exons 2-19 in
RT   dystrophin gene.";
RL   Stem Cell Res. 53:102298-102298(2021).
//