학술논문

Rare pathogenic variants in WNK3 cause X-linked intellectual disability
Document Type
Journal
Author
Kury, SebastienZhang, JinweiBesnard, ThomasCaro-Llopis, AlfonsoZeng, XueRobert, Stephanie M.Josiah, Sunday S.Kiziltug, EmreDenomme-Pichon, Anne-SophieCogne, BenjaminKundishora, Adam J.Hao, Le T.Li, HongStevenson, Roger E.Louie, Raymond J.Deb, WallidTorti, ErinVignard, VirginieMcWalter, KirstyRaymond, F. LucyRajabi, FarrahRanza, EmmanuelleGrozeva, DetelinaCoury, Stephanie A.Blanc, XavierBrischoux-Boucher, EliseKeren, BorisOunap, KatrinReinson, KaritIlves, PilviWentzensen, Ingrid M.Barr, Eileen E.Guihard, Solveig HeideCharles, PerrineSeaby, Eleanor G.Monaghan, Kristin G.Rio, Marlenevan Bever, Yolandevan Slegtenhorst, MarjonChung, Wendy K.Wilson, AshleyQuinquis, DelphineBreheret, FloraRetterer, KyleLindenbaum, PierreScalais, EmmanuelRhodes, LindsayStouffs, KatrienPereira, Elaine M.Berger, Sara M.Milla, Sarah S.Jaykumar, Ankita B.Cobb, Melanie H.Panchagnula, ShreyasDuy, Phan Q.Vincent, MarieMercier, SandraGilbert-Dussardier, BrigitteLe Guillou, XavierAudebert-Bellanger, SeverineOdent, SylvieSchmitt, SebastienBoisseau, PierreBonneau, DominiqueToutain, AnnickColin, EstellePasquier, LaurentRedon, RichardBouman, ArjanRosenfeld, Jill A.Friez, Michael J.Perez-Pena, HelenaRizvi, Syed Raza AkhtarHaider, ShozebAntonarakis, Stylianos E.Schwartz, Charles E.Martinez, FranciscoBezieau, StephaneKahle, Kristopher T.Isidor, Bertrand
Source
GENETICS IN MEDICINE; SEP 2022, 24 9, p1941-p1951, 11p.
Subject
Language
English
ISSN
15300366