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Defective Mismatch Repair Associated With PMS2
An instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-5632987)
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Statements
instance of
biological pathway
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5632987
part of
Diseases of Mismatch Repair (MMR)
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5632987
found in taxon
Homo sapiens
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5632987
exact match
https://identifiers.org/reactome:R-HSA-5632987
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5632987
has part(s)
PMS2 variants-defective DNA mismatch repair
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5632987
cites work
The molecular basis of Turcot's syndrome
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5632987
Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome).
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5632987
Identifiers
Reactome ID
R-HSA-5632987
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-5632987
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