Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality

Lam M, Moslem M, Bryois J, Pronk RJ, Uhlin E, Ellström ID, Laan L, Olive J, Morse R, Rönnholm H, Louhivuori L, Korol SV, Dahl N, Uhlén P, Anderlid BM, Kele M, Sullivan PF, Falk A

Experimental Cell Research - (-) 111469 [2019-07-00; online 2019-07-00]

Eukaryotic Single Cell Genomics (ESCG) [Service]

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DOI 10.1016/j.yexcr.2019.06.014

Crossref 10.1016/j.yexcr.2019.06.014