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(Q93553991)
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FINCBi001-A
cell line
F56L cl33
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Statements
instance of
cell line
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_YD66
Induced pluripotent stem cell line
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_YD66
described by source
Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON)
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_YD66
established from medical condition
Leber hereditary optic neuropathy
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_YD66
derived from organism type
Homo sapiens
sex or gender
female
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_YD66
Identifiers
Cellosaurus ID
CVCL_YD66
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_YD66
hPSCreg cell line ID
FINCBi001-A
1 reference
stated in
Cellosaurus release 44
retrieved
8 January 2023
Cellosaurus ID
CVCL_YD66
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