Associated Papers
Single-strand mismatch and damage patterns revealed by single-molecule DNA sequencing.
Liu MH et al.
Biorxiv : the Preprint Server for Biology, 2023
36824744 (PubMed )
Supplement: media-3.xlsx › Suppl_Table_1_-_Samples
Carrier testing for severe childhood recessive diseases by next-generation sequencing.
Bell CJ et al.
Science Translational Medicine, 2011
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome.
Laugel V et al.
Human Mutation, 2010
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