Associated Papers
An X-Linked Ataxia Syndrome in a Family with Hearing Loss Associated with a Novel Variant in the BCAP31 Gene.
Paucar M et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2025
39831730 (PubMed )
Supplement: MDS-40-672-s005.pdf
Structural insights into the duplex DNA processing of TREX2.
Cheng HL et al.
Nucleic Acids Research, 2018
Multifaceted role of TREX2 in the skin defense against UV-induced skin carcinogenesis.
Manils J et al.
Oncotarget, 2015
Biochemical and cellular characteristics of the 3' -> 5' exonuclease TREX2.
Chen MJ et al.
Nucleic Acids Research, 2007
Sequence variants in the 3'-->5' deoxyribonuclease TREX2: identification in a genetic screen and effects on catalysis by the recombinant proteins.
Perrino FW et al.
Advances in Enzyme Regulation, 2004
Select a paper to view details