Mutation-Specific Pathophysiological Mechanisms In A New Satb1-Associated Neurodevelopmental Disorder
J. Den Hoed,E. De Boer,N. Voisin,N. Guex,L. Snijders Blok,J. Chrast,L. Manwaring,M. Willing,A. Waheeb,M. Osmond,K. Mcwalter,A. Vitobello,F. Demurger,A. Lavillaureix,S. Odent, B. Mazel,L. Faivre,I. Thiffault, C. Schwager,S. M. Amudhavalli,J. A. Rosenfeld, K. Radtke,E. Preiksaitiene,E. Ranza,C. Depienne,A. Kuechler,S. Mohammed, Y. Hamzavi Abedi, V. R. Bonagura, B. Zuccarelli, B. Horist, V. Krishnamurthy, A. A. Kattentidt-Mouravieva, L. Granger, A. Petersen, K. L. Jones,M. Sinnema,A. P. A. Stegmann,R. Newbury-Ecob,U. Kini,D. F. Newbury,C. Gilissen,H. Brunner,T. Kleefstra,A. Reymond,L. E. L. M. Vissers,S. E. Fisher EUROPEAN JOURNAL OF HUMAN GENETICS(2020)
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