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. |
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| 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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| ISSN: | 0931041X |
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| DOI: | 10.1007/s00467-025-06787-1 |
