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Data from: 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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posted on 21.02.2019, 00:00 by Matti Lam, Malin Kele, Marcela Ferella, Anna Juréus, Peter Lönnerberg, Anna Falk
Single cell RNA STRT-seq data generated on C1 Fluidigm platform from iPS cell derived neural stem cells and neuronal differentitated cells. Data includes single cell transcriptomes from two human individuals, one healthy control individual and one Autism Spectrum Disorder diagnosed individual with bi-allelic NRXN1-alpha deletion.

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Karolinska institutet

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datacentre@scilifelab.se

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