English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

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

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.

Item is

Files

show Files

Locators

show

Creators

show
hide
 Creators:
Tschernoster, Nikolai, Author
Erger, Florian, Author
Kohl, Stefan, Author
Reusch, Björn, Author
Wenzel, Andrea, Author
Walsh, Stephen, Author
Thiele, Holger, Author
Becker, Christian, Author
Franitza, Marek, Author
Bartram, Malte P., Author
Kömhoff, Martin, Author
Schumacher, A. L.1, Author           
Kukat, C.1, Author           
Borodina, Tatiana, Author
Quedenau, Claudia, Author
Nürnberg, Peter, Author
Rinschen, Markus M, Author
Driller, Jan H., Author
Pedersen, Bjørn P., Author
Schlingmann, Karl P., Author
Hüttel, Bruno, AuthorBockenhauer, Detlef, AuthorBeck, Bodo, AuthorAltmüller, Janine, Author more..
Affiliations:
1FACS & Imaging, Core Facilities, Max Planck Institute for Biology of Ageing, Max Planck Society, ou_1942304              

Content

show

Details

show
hide
Language(s):
 Dates: 2023-08-23
 Publication Status: Published online
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1186/s13073-023-01215-1
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Genome Medicine
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 15 Sequence Number: 62 Start / End Page: - Identifier: ISSN: 1756-994X