Long‐read nanopore sequencing resolves a TMEM231 gene conversion event causing Meckel–Gruber syndrome

Watson, CM orcid.org/0000-0003-2371-1844, Dean, P, Camm, N et al. (4 more authors) (2020) Long‐read nanopore sequencing resolves a TMEM231 gene conversion event causing Meckel–Gruber syndrome. Human Mutation, 41 (2). pp. 525-531. ISSN 1059-7794

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Authors/Creators:
Copyright, Publisher and Additional Information: © 2019 Wiley Periodicals, Inc. This is the peer reviewed version of the following article: Watson, CM, Dean, P, Camm, N, et al. Long‐read nanopore sequencing resolves a TMEM231 gene conversion event causing Meckel–Gruber syndrome. Human Mutation. 2019; 1– 7. https://doi.org/10.1002/humu.23940, which has been published in final form at https://doi.org/10.1002/humu.23940. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving. Uploaded in accordance with the publisher's self-archiving policy.
Keywords: gene conversion; Meckel–Gruber syndrome; nanopore sequencing; TMEM231
Dates:
  • Published: February 2020
  • Accepted: 28 October 2019
  • Published (online): 30 October 2019
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > Institute of Molecular Medicine (LIMM) (Leeds) > Section of Opthalmology and Neurosciences (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 26 Nov 2019 15:57
Last Modified: 21 Jan 2020 09:58
Status: Published
Publisher: Wiley
Identification Number: https://doi.org/10.1002/humu.23940
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