Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality.
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P. Sullivan | J. Bryois | P. Uhlén | B. Anderlid | N. Dahl | S. Korol | A. Falk | Malin Kele | M. Moslem | L. Louhivuori | Elias Uhlin | Matti Lam | Jessica F. Olive | Loora Laan | H. Roennholm | R. Pronk | Ivar Dehnisch Ellström | Rebecca Morse | Anna Falk