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Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.
J Clin Invest. 2020 Jan 2;130(1):335-344. doi: 10.1172/JCI129937.
J Clin Invest. 2020.
PMID: 31613795
Free PMC article.
Clinical Trial.
Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.
Bedin M, Boyer O, Servais A, Li Y, Villoing-Gaudé L, Tête MJ, Cambier A, Hogan J, Baudouin V, Krid S, Bensman A, Lammens F, Louillet F, Ranchin B, Vigneau C, Bouteau I, Isnard-Bagnis C, Mache CJ, Schäfer T, Pape L, Gödel M, Huber TB, Benz M, Klaus G, Hansen M, Latta K, Gribouval O, Morinière V, Tournant C, Grohmann M, Kuhn E, Wagner T, Bole-Feysot C, Jabot-Hanin F, Nitschké P, Ahluwalia TS, Köttgen A, Andersen CBF, Bergmann C, Antignac C, Simons M.
Bedin M, et al. Among authors: tournant c.
J Clin Invest. 2022 Jun 1;132(11):e161852. doi: 10.1172/JCI161852.
J Clin Invest. 2022.
PMID: 35642643
Free PMC article.
No abstract available.
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Cystic kidney diseases associated with mutations in phosphomannomutase 2 promotor: a large spectrum of phenotypes.
Dorval G, Jeanpierre C, Morinière V, Tournant C, Bessières B, Attié-Bittach T, Amiel J, Spaggari E, Ville Y, Merieau E, Gubler MC, Saunier S, Heidet L.
Dorval G, et al. Among authors: tournant c.
Pediatr Nephrol. 2021 Aug;36(8):2361-2369. doi: 10.1007/s00467-021-04953-9. Epub 2021 Feb 13.
Pediatr Nephrol. 2021.
PMID: 33580824
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Targeted next-generation sequencing in a large series of fetuses with severe renal diseases.
Jordan P, Dorval G, Arrondel C, Morinière V, Tournant C, Audrezet MP, Michel-Calemard L, Putoux A, Lesca G, Labalme A, Whalen S, Loeuillet L, Martinovic J, Attie-Bitach T, Bessières B, Schaefer E, Scheidecker S, Lambert L, Beneteau C, Patat O, Boute-Benejean O, Molin A, Guimiot F, Fontanarosa N, Nizon M, Lefebvre M, Jeanpierre C, Saunier S, Heidet L.
Jordan P, et al. Among authors: tournant c.
Hum Mutat. 2022 Mar;43(3):347-361. doi: 10.1002/humu.24324. Epub 2022 Jan 10.
Hum Mutat. 2022.
PMID: 35005812
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