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(Q54993975)
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WG2290
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_QZ36
finite cell line
1 reference
stated in
Cellosaurus release 49
retrieved
15 July 2024
Cellosaurus ID
CVCL_QZ36
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_QZ36
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_QZ36
established from medical condition
Arakawa's syndrome II
1 reference
stated in
Cellosaurus release 49
retrieved
15 July 2024
Cellosaurus ID
CVCL_QZ36
derived from organism type
Homo sapiens
sex or gender
male
1 reference
stated in
Cellosaurus release 49
retrieved
15 July 2024
Cellosaurus ID
CVCL_QZ36
Identifiers
Cellosaurus ID
CVCL_QZ36
1 reference
stated in
Cellosaurus release 49
retrieved
15 July 2024
Cellosaurus ID
CVCL_QZ36
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