Biallelic <i>RXFP2</i> variants lead to congenital bilateral cryptorchidism and male infertility, supporting a role of RXFP2 in spermatogenesis

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Publication Details

Journal
Human Reproduction
Published
2024-09-02
DOI
https://doi.org/10.1093/humrep/deae195
Citations
5
Primary Topic
Pregnancy-related medical research
Type
article
Field-Weighted Citation Impact
2.71

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article

Biallelic RXFP2 variants lead to congenital bilateral cryptorchidism and male infertility, supporting a role of RXFP2 in spermatogenesis

Julie Van De Velde, Andrew J. Sinclair, Hannah Verdin, Hannes Syryn et al.
5 citations
Human Reproduction
Pregnancy-related medical research
2.71
article

Biallelic RXFP2 variants lead to congenital bilateral cryptorchidism and male infertility, supporting a role of RXFP2 in spermatogenesis

Julie Van De Velde, Andrew J. Sinclair, Hannah Verdin, Hannes Syryn, Griet De Clercq, Frank Peelman, Ross A. D. Bathgate, Elfride De Baere, Katie Ayers, Annelies Dheedene, Martine Cools
article en
5 citations

Abstract

No abstract available for this paper.
Human ReproductionVol. 39(10)
HOGENT University of Applied Sciences and Arts (BE), Royal Children's Hospital (AU), The University of Melbourne (AU), Florey Institute of Neuroscience and Mental Health (AU), Ghent University Hospital (BE), Ghent University (BE), Murdoch Children's Research Institute (AU)
Fonds Wetenschappelijk Onderzoek
Good health and well-being
Openalex Percentile: Top 10%
Pregnancy-related medical research
2.71
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