| Cell line name | DMBi001-A-1 |
|---|---|
| Accession | CVCL_A7LC |
| Resource Identification Initiative | To cite this cell line use: DMBi001-A-1 (RRID:CVCL_A7LC) |
| Comments | From: Department of Medical Biotechnology, Jagiellonian University; Krakow; Poland. Population: Caucasian. Knockout cell: Method=CRISPR/Cas9; HGNC; 6482; LAMA2. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Merosin-deficient congenital muscular dystrophy type 1A (NCIt: C118783) Laminin subunit alpha 2-related congenital muscular dystrophy (ORDO: Orphanet_258) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_ZC40 (DMBi001-A) |
| Sex of cell | Male |
| Age at sampling | 58Y |
| Category | Induced pluripotent stem cell |
| Publications | PubMed=34509921; DOI=10.1016/j.scr.2021.102529 |
| Cross-references | |
| Cell line databases/resources | hPSCreg; DMBi001-A-1 |
| Biological sample resources | BioSamples; SAMEA8770928 |
| Encyclopedic resources | Wikidata; Q107114814 |
| Entry history | |
| Entry creation | 20-May-2021 |
| Last entry update | 29-Jun-2023 |
| Version number | 4 |