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Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders

Lookup NU author(s): Dr Brendan Houston, Ludmila Volo┼żonoka, Francesco Kumara Mastrorosa, Dr Giles Holt, Dr Bilal AlobaidiORCiD, Professor Joris VeltmanORCiD, Dr Harsh Sheth



This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).

Publication metadata

Author(s): Oud MS, Houston BJ, Volozonoka L, Mastrorosa FK, Holt GS, Alobaidi BKS, deVries PF, Astuti G, Ramos L, Mclachlan RI, O'Bryan MK, Veltman JA, Chemes HE, Sheth H

Publication type: Article

Publication status: Published

Journal: Human Reproduction

Year: 2021

Volume: 36

Issue: 9

Pages: 2597-2611

Print publication date: 01/09/2021

Online publication date: 05/06/2021

Acceptance date: 07/04/2021

Date deposited: 30/07/2021

ISSN (print): 0268-1161

ISSN (electronic): 1460-2350

Publisher: Oxford University Press


DOI: 10.1093/humrep/deab099


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Funder referenceFunder name
Australian National Health
Investigator Award in Science from the Wellcome Trust (209451)
National Research Council of Argentina (PIP 0900 and 4584)
WM160091Royal Society
The Netherlands Organisation for Scientific Research (918-15-667)