Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

Author:

den Hoed Joery,de Boer Elke,Voisin Norine,Dingemans Alexander J.M.,Guex Nicolas,Wiel Laurens,Nellaker Christoffer,Amudhavalli Shivarajan M.,Banka Siddharth,Bena Frederique S.,Ben-Zeev Bruria,Bonagura Vincent R.,Bruel Ange-Line,Brunet Theresa,Brunner Han G.,Chew Hui B.,Chrast Jacqueline,Cimbalistienė Loreta,Coon Hilary,Délot Emmanuèlle C.,Démurger Florence,Denommé-Pichon Anne-Sophie,Depienne Christel,Donnai Dian,Dyment David A.,Elpeleg Orly,Faivre Laurence,Gilissen Christian,Granger Leslie,Haber Benjamin,Hachiya Yasuo,Abedi Yasmin Hamzavi,Hanebeck Jennifer,Hehir-Kwa Jayne Y.,Horist Brooke,Itai Toshiyuki,Jackson Adam,Jewell Rosalyn,Jones Kelly L.,Joss Shelagh,Kashii Hirofumi,Kato Mitsuhiro,Kattentidt-Mouravieva Anja A.,Kok Fernando,Kotzaeridou Urania,Krishnamurthy Vidya,Kučinskas Vaidutis,Kuechler Alma,Lavillaureix Alinoë,Liu Pengfei,Manwaring Linda,Matsumoto Naomichi,Mazel Benoît,McWalter Kirsty,Meiner Vardiella,Mikati Mohamad A.,Miyatake Satoko,Mizuguchi Takeshi,Moey Lip H.,Mohammed Shehla,Mor-Shaked Hagar,Mountford Hayley,Newbury-Ecob Ruth,Odent Sylvie,Orec Laura,Osmond Matthew,Palculict Timothy B.,Parker Michael,Petersen Andrea K.,Pfundt Rolph,Preikšaitienė Eglė,Radtke Kelly,Ranza Emmanuelle,Rosenfeld Jill A.,Santiago-Sim Teresa,Schwager Caitlin,Sinnema Margje,Snijders Blok Lot,Spillmann Rebecca C.,Stegmann Alexander P.A.,Thiffault Isabelle,Tran Linh,Vaknin-Dembinsky Adi,Vedovato-dos-Santos Juliana H.,Schrier Vergano Samantha A.,Vilain Eric,Vitobello Antonio,Wagner Matias,Waheeb Androu,Willing Marcia,Zuccarelli Britton,Kini Usha,Newbury Dianne F.,Kleefstra Tjitske,Reymond Alexandre,Fisher Simon E.,Vissers Lisenka E.L.M.

Funder

Max-Planck-Gesellschaft

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference30 articles.

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