| Bibliographic Citation
| - Zhang Jinwei, Besnard Thomas, Denommé-Pichon Anne-Sophie, Cogné Benjamin, Louie Raymond, Torti Erin, Vignard Virginie, Mcwalter Kirsty, Brischoux-Boucher Elise, Keren Boris, Guihard Solveig Heide, Rio Marlène, Quinquis Delphine, Mercier Sandra, Gilbert-Dussardier Brigitte, Le Guillou Xavier, Audebert-Bellanger Séverine, Odent Sylvie, Schmitt Sébastien, Boisseau Pierre, Bonneau Dominique, Toutain Annick, Colin Estelle, Pasquier Laurent, Redon Richard, Antonarakis Stylianos, Schwartz Charles, Bézieau Stéphane, Isidor Bertrand . Rare pathogenic variants in WNK3 cause X-linked intellectual disability . Genetics in Medicine, 2022, 24 (9), pp.1941-1951 . ⟨10.1016/j.gim.2022.05.009⟩
- Zhang Jinwei, Besnard Thomas, Caro-Llopis Alfonso, Zeng Xue, Robert Stephanie, Josiah Sunday, Kiziltug Emre, Denommé-Pichon Anne-Sophie, Cogné Benjamin, Kundishora Adam, Hao Le, Li Hong, Stevenson Roger, Louie Raymond, Deb Wallid, Torti Erin, Vignard Virginie, Mcwalter Kirsty, Raymond F Lucy, Rajabi Farrah, Ranza Emmanuelle, Grozeva Detelina, Coury Stephanie, Blanc Xavier, Brischoux-Boucher Elise, Keren Boris, Õunap Katrin, Reinson Karit, Ilves Pilvi, Wentzensen Ingrid, Barr Eileen, Guihard Solveig Heide, Charles Perrine, Seaby Eleanor, Monaghan Kristin, Rio Marlène, van Bever Yolande, van Slegtenhorst Marjon, Chung Wendy, Wilson Ashley, Quinquis Delphine, Bréhéret Flora, Retterer Kyle, Lindenbaum Pierre, Scalais Emmanuel, Rhodes Lindsay, Stouffs Katrien, Pereira Elaine, Berger Sara, Milla Sarah, Jaykumar Ankita, Cobb Melanie, Panchagnula Shreyas, Duy Phan, Vincent Marie, Mercier Sandra, Gilbert-Dussardier Brigitte, Le Guillou Xavier, Audebert-Bellanger Séverine, Odent Sylvie, Schmitt Sébastien, Boisseau Pierre, Bonneau Dominique, Toutain Annick, Colin Estelle, Pasquier Laurent, Redon Richard, Bouman Arjan, Rosenfeld Jill, Friez Michael, Pérez-Peña Helena, Akhtar Rizvi Syed Raza, Haider Shozeb, Antonarakis Stylianos, Schwartz Charles, Martínez Francisco, Bézieau Stéphane, Isidor Bertrand . Rare pathogenic variants in WNK3 cause X-linked intellectual disability . Genetics in Medicine, 2022, 24 (9), pp.1941-1951 . ⟨10.1016/j.gim.2022.05.009⟩
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