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(Q54993936)
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WG1892
cell line
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Statements
instance of
cell line
1 reference
stated in
Cellosaurus release 49
retrieved
15 July 2024
Cellosaurus ID
CVCL_QZ35
finite cell line
1 reference
stated in
Cellosaurus release 49
retrieved
15 July 2024
Cellosaurus ID
CVCL_QZ35
described by source
Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders
1 reference
stated in
Cellosaurus release 49
retrieved
15 July 2024
Cellosaurus ID
CVCL_QZ35
Defects in auxiliary redox proteins lead to functional methionine synthase deficiency
1 reference
stated in
Cellosaurus release 49
retrieved
15 July 2024
Cellosaurus ID
CVCL_QZ35
established from medical condition
Arakawa's syndrome II
1 reference
stated in
Cellosaurus release 49
retrieved
15 July 2024
Cellosaurus ID
CVCL_QZ35
derived from organism type
Homo sapiens
sex or gender
male
1 reference
stated in
Cellosaurus release 49
retrieved
15 July 2024
Cellosaurus ID
CVCL_QZ35
Identifiers
Cellosaurus ID
CVCL_QZ35
1 reference
stated in
Cellosaurus release 49
retrieved
15 July 2024
Cellosaurus ID
CVCL_QZ35
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