| Cell line name | HPS1066 |
|---|---|
| Accession | CVCL_UN57 |
| Resource Identification Initiative | To cite this cell line use: HPS1066 (RRID:CVCL_UN57) |
| Comments | Population: Japanese. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Congenital myasthenic syndrome (NCIt: C84647) Congenital myasthenic syndrome (ORDO: Orphanet_590) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_UP78 ! HPS1067 CVCL_UP79 ! HPS1068 CVCL_UP80 ! HPS1069 CVCL_UP81 ! HPS1070 |
| Sex of cell | Male |
| Age at sampling | 10-19Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS1066 |
| Encyclopedic resources | Wikidata; Q94219464 |
| Entry history | |
| Entry creation | 25-Feb-2019 |
| Last entry update | 29-Jun-2023 |
| Version number | 5 |