ADGRL1 haploinsufficiency causes a variable spectrum of neurodevelopmental disorders in humans and in a mouse model with altered synaptic activity
Antonio Vitobello,Benoit Mazel,Vera G. Lelianova,Alice Zangrandi, Evelina Petitto,Jason Suckling,Vincenzo Salpietro,Robert Meyer,Miriam Elbracht,Ingo Kurth,Thomas Eggermann,Ouafa Benlaouer,Gurprit S. Lall, Alexander Tonevitsky,Daryl Scott,Katie M. Chan,Jill A. Rosenfeld,Sophie Nambot,Hana Safraou,Ange-Line Bruel,Anne-Sophie Denomme-Pichon,Frederic Tran Mau-Them,Christophe Philippe,Yannis Duf-Fourd,Hui Guo,Andrea Petersen,Leslie Granger,Amy Crunk,Allan Bayat,Pasquale Striano, Federico Zara,Marcello Scala,Quentin Thomas,Andree Delahaye,Jean-Madeleine de Sainte Agathe,Julien Buratti,Serguei Kozlov,Laurence Faivre,Christel Thauvin-Robinet,Yuri Ushkaryov EUROPEAN JOURNAL OF HUMAN GENETICS(2023)
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