ID   BGUi009-A
AC   CVCL_A4ZM
SY   DCM-O1; DCM-O
DR   BioSamples; SAMEA8093253
DR   hPSCreg; BGUi009-A
DR   Wikidata; Q107113456
RX   PubMed=34088011;
CC   From: Ben Gurion University of the Negev; Beer Sheva; Israel.
CC   Population: Bedouin.
CC   Sequence variation: Mutation; HGNC; 29131; PLEKHM2; Simple; p.Lys645Alafs*12 (c.1932_1933delAG) (c.2156_2157delAG); ClinVar=VCV000253148; Zygosity=Homozygous (PubMed=34088011).
CC   Derived from site: In situ; Connective tissue; UBERON=UBERON_0002384.
DI   NCIt; C99544; Left ventricular non-compaction syndrome
DI   ORDO; Orphanet_54260; Left ventricular noncompaction
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_A8XF ! BGUi009-B
SX   Male
AG   13Y
CA   Induced pluripotent stem cell
DT   Created: 20-05-21; Last updated: 29-06-23; Version: 4
//
RX   PubMed=34088011; DOI=10.1016/j.scr.2021.102382;
RA   Ben-Zvi H., Korover N., Rabinski T., Ofir R., Cohen S.;
RT   "Generation and characterization of three human induced pluripotent
RT   stem cell lines (iPSC) from two family members with dilated
RT   cardiomyopathy and left ventricular noncompaction (DCM-LVNC) and one
RT   healthy heterozygote sibling.";
RL   Stem Cell Res. 53:102382-102382(2021).
//