SAMEA104130970

UCLi006-A

Released on 2017 / 12 / 06 00:00:00 UTC
Updated on 2019 / 07 / 24 13:40:34 UTC

Attributes

Type Value
cell type induced pluripotent stem cell
disease state Congenital muscular dystrophy due to LMNA mutation
donor id SAMEA104130971
material cell line
organism Homo sapiens
phenotype EFO_0004905;Orphanet_157973
project EBiSC
sex male
submission description 1 Homo sapiens samples from hPSCreg
submission identifier GSB-3006
submission title 1 Homo sapiens samples from hPSCreg
synonym LCMD-L302P-UCL01C2

Relationships

Source Type Target
SAMEA104130970 derived from SAMEA104130971
SAMEG4750483 has member SAMEA104130970

External Links