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(Q94318004)
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INMi004-A
cell line
CRX-LCA-iPSC
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Statements
instance of
cell line
1 reference
stated in
Cellosaurus release 44
retrieved
23 January 2023
Cellosaurus ID
CVCL_WR02
Induced pluripotent stem cell line
1 reference
stated in
Cellosaurus release 44
retrieved
23 January 2023
Cellosaurus ID
CVCL_WR02
described by source
Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis
1 reference
stated in
Cellosaurus release 44
retrieved
23 January 2023
Cellosaurus ID
CVCL_WR02
established from medical condition
Leber congenital amaurosis
1 reference
stated in
Cellosaurus release 44
retrieved
23 January 2023
Cellosaurus ID
CVCL_WR02
derived from organism type
Homo sapiens
sex or gender
male
1 reference
stated in
Cellosaurus release 44
retrieved
23 January 2023
Cellosaurus ID
CVCL_WR02
Identifiers
Cellosaurus ID
CVCL_WR02
1 reference
stated in
Cellosaurus release 44
retrieved
23 January 2023
Cellosaurus ID
CVCL_WR02
hPSCreg cell line ID
INMi004-A
1 reference
stated in
Cellosaurus release 44
retrieved
23 January 2023
Cellosaurus ID
CVCL_WR02
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