Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality
Titel:
Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality
Auteur:
Lam, Matti Moslem, Mohsen Bryois, Julien Pronk, Robin J. Uhlin, Elias Ellström, Ivar Dehnisch Laan, Loora Olive, Jessica Morse, Rebecca Rönnholm, Harriet Louhivuori, Lauri Korol, Sergiy V. Dahl, Niklas Uhlén, Per Anderlid, Britt-Marie Kele, Malin Sullivan, Patrick F. Falk, Anna