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MBNL2 dysfunction in outer radial glial cells is associated with disrupted corticogenesis in congenital myotonic dystrophy

GSE317529 Homo sapiens Other; Expression profiling by high throughput sequencing 15 samples Submitted 2026/03/12 Platform GPL24676
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Published in
MBNL2 dysfunction in outer radial glial cells is associated with disrupted corticogenesis in congenital myotonic dystrophy
De Serres-Bérard T, Gosztyla ML, Nguyen G et al. · Neurobiology of disease 2026 · PMID 41644016 · doi:10.1016/j.nbd.2026.107305
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Direct links to NCBI, no account and no request form: the whole study as GSE317529_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 15 samples. Raw sequencing reads are also available from ENA.

Also filed as BioProject PRJNA1414420 and SRA study SRP658373. Searching any of these in the dataset finder brings you back here.

Study design
12 conditions, each sampled once — no replicated groups
70-day-old forebrain organoids, unaffected co… ×2 70-day-old forebrain organoids, congenital my… ×2 70-day-old forebrain organoids, isogenic cont… ×2

Read from 15 sample titles: 12 distinct titles with little repetition. Check it against the sample list below before relying on it.

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