CUX1-related Neurodevelopmental Disorder: Deep Insights into Phenotype-Genotype Spectrum and Underlying Pathology
Henry Oppermann, Elia Marcos-Grañeda,Linnea A. Weiss,Christina A. Gurnett,Anne Marie Jelsig, Susanne H. Vineke,Bertrand Isidor,Sandra Mercier,Kari Magnussen,Pia Zacher,Mona Hashim,Alistair T. Pagnamenta,Simone Race,Siddharth Srivastava,Zoë Frazier,Robert Maiwald,Matthias Pergande,Donatella Milani,Martina Rinelli,Jonathan Levy,Ilona Krey,Paolo Fontana,Fortunato Lonardo, Stephanie Riley, Jasmine Kretzer,Julia Rankin,Linda M. Reis,Elena V. Semina,Miriam S. Reuter,Stephen W. Scherer,Maria Iascone,Denisa Weis,Christina R. Fagerberg,Charlotte Brasch-Andersen,Lars Kjaersgaard Hansen,Alma Kuechler,Nathan Noble,Alice Gardham,Jessica Tenney,Geetanjali Rathore,Stefanie Beck-Woedl,Tobias B. Haack, Despoina C. Pavlidou,Isis Atallah,Julia Vodopiutz,Andreas R. Janecke,Tzung-Chien Hsieh,Hellen Lesmann,Hannah Klinkhammer,Peter M. Krawitz,Johannes R. Lemke,Rami Abou Jamra,Marta Nieto,Zeynep Tümer,Konrad Platzer EUROPEAN JOURNAL OF HUMAN GENETICS（2023）
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Gene Expression Regulation
AI 理解论文
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