Long-read sequencing identifies a common transposition haplotype predisposing 
for CLCNKB deletions

Tschernoster, Nikolai; Erger, Florian; Kohl, Stefan; Reusch, Björn; Wenzel, Andrea; Walsh, Stephen; Thiele, Holger; Becker, Christian; Franitza, Marek; Bartram, Malte P.; Kömhoff, Martin; Schumacher, A. L.; Kukat, C.; Borodina, Tatiana; Quedenau, Claudia; Nürnberg, Peter; Rinschen, Markus M; Driller, Jan H.; Pedersen, Bjørn P.; Schlingmann, Karl P.; Hüttel, Bruno; Bockenhauer, Detlef; Beck, Bodo; Altmüller, Janine

doi:10.1186/s13073-023-01215-1

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Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions

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Schumacher, A. L.
FACS & Imaging, Core Facilities, Max Planck Institute for Biology of Ageing, Max Planck Society;

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Kukat, C.
FACS & Imaging, Core Facilities, Max Planck Institute for Biology of Ageing, Max Planck Society;

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Tschernoster, N., Erger, F., Kohl, S., Reusch, B., Wenzel, A., Walsh, S., et al. (2023). Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions. Genome Medicine, 15: 62. doi:10.1186/s13073-023-01215-1.

Cite as: https://hdl.handle.net/21.11116/0000-000D-A11F-B

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