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Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninism

Crossref DOI link: https://doi.org/10.1007/s00467-025-06787-1

Published Online: 2025-05-14

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Marsili, Luisa

Mantecon, Matthieu

Arrondel, Christelle

Barcia, Giulia

Assouline, Zahra

Gribouval, Olivier

Wellesley, Diana

Harrison, Victoria

Marijon, Pierre

Colson, Cindy

Stichelbout, Morgane

Gubler, Marie-Claire

Antignac, Corinne

Rotig, Agnes

Heidet, Laurence https://orcid.org/0000-0002-1362-5515
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Text and Data Mining valid from 2025-05-14

Version of Record valid from 2025-05-14
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Article History

Received: 20 February 2025

Revised: 28 March 2025

Accepted: 31 March 2025

First Online: 14 May 2025

Declarations

:

: The authors declare no competing interests.

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