Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions
长读测序鉴定出一种常见的易导致 CLCNKB 缺失的转座单倍型
期刊:Genome Medicine
影响因子:10.4
doi:10.1186/s13073-023-01215-1
Nikolai Tschernoster, Florian Erger, Stefan Kohl, Björn Reusch, Andrea Wenzel, Stephen Walsh, Holger Thiele, Christian Becker, Marek Franitza, Malte P Bartram, Martin Kömhoff, Lena Schumacher, Christian Kukat, Tatiana Borodina, Claudia Quedenau, Peter Nürnberg, Markus M Rinschen, Jan H Driller, Bjør