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Long-read sequencing identifies a common transposition hapl..:

Tschernoster, Nikolai ; Erger, Florian ; Kohl, Stefan...
https://pure.au.dk/portal/da/publications/longread-sequencing-identifies-a-common-transposition-haplotype-predisposing-for-clcnkb-deletions(53efb788-2420-4d57-8613-b7821ec186cc).html. , 2023

Link: https://pure.au.dk/portal/da/publications/longread-seq..

RT Journal
T1 <Title>Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftuniaarhuspubl:oai:pure.atira.dk:publications_53efb788-2420-4d57-8613-b7821ec186cc&Exemplar=1&LAN=DE
				
A1 Tschernoster, Nikolai
A1 Erger, Florian
A1 Kohl, Stefan
A1 Reusch, Björn
A1 Wenzel, Andrea
A1 Walsh, Stephen
A1 Thiele, Holger
A1 Becker, Christian
A1 Franitza, Marek
A1 Bartram, Malte P
A1 Kömhoff, Martin
A1 Schumacher, Lena
A1 Kukat, Christian
A1 Borodina, Tatiana
A1 Quedenau, Claudia
A1 Nürnberg, Peter
A1 Rinschen, Markus M
A1 Driller, Jan H
A1 Pedersen, Bjørn P
A1 Schlingmann, Karl P
A1 Hüttel, Bruno
A1 Bockenhauer, Detlef
A1 Beck, Bodo
A1 Altmüller, Janine
YR 2023
K1 Bartter syndrome type 3
K1 CLCNKA
K1 CLCNKB
K1 HiFi-sequencing
K1 Long-read sequencing
K1 Next-generation sequencing
K1 Risk haplotype
K1 Salt-wasting tubulopathy
K1 Structural variant
K1 Target enrichment
JF https://pure.au.dk/portal/da/publications/longread-sequencing-identifies-a-common-transposition-haplotype-predisposing-for-clcnkb-deletions(53efb788-2420-4d57-8613-b7821ec186cc).html
LK http://dx.doi.org/https://pure.au.dk/portal/da/publications/longread-sequencing-identifies-a-common-transposition-haplotype-predisposing-for-clcnkb-deletions(53efb788-2420-4d57-8613-b7821ec186cc).html
DO https://pure.au.dk/portal/da/publications/longread-sequencing-identifies-a-common-transposition-haplotype-predisposing-for-clcnkb-deletions(53efb788-2420-4d57-8613-b7821ec186cc).html
SF ELIB - SuUB Bremen

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