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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.

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Title: Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninism.
Authors: Marsili, Luisa1,2, Mantecon, Matthieu3, Arrondel, Christelle4, Barcia, Giulia3,5, Assouline, Zahra5, Gribouval, Olivier4, Wellesley, Diana6, Harrison, Victoria6, Marijon, Pierre7, Colson, Cindy1, Stichelbout, Morgane8, Gubler, Marie-Claire4, Antignac, Corinne4, Rotig, Agnes3, Heidet, Laurence4,7,9 laurence.heidet@aphp.fr
Source: Pediatric Nephrology. Sep2025, Vol. 40 Issue 9, p2823-2828. 6p.
Database: Academic Search Ultimate
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  Data: Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninism.
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  Data: <searchLink fieldCode="JN" term="%22Pediatric+Nephrology%22">Pediatric Nephrology</searchLink>. Sep2025, Vol. 40 Issue 9, p2823-2828. 6p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=186910321
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        Value: 10.1007/s00467-025-06787-1
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      – Code: eng
        Text: English
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        PageCount: 6
        StartPage: 2823
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      – TitleFull: Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninism.
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              M: 09
              Text: Sep2025
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              Y: 2025
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