Clinical and molecular characterization of a novel LMX1A frameshift mutation near the C-terminus lead to familial non-syndromic sensorineural hearing loss
Direct links to NCBI, no account and no request form: the whole study as GSE200599_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 9 samples. Raw sequencing reads are also available from ENA.
Also filed as BioProject PRJNA825501 and SRA study SRP369491. Searching any of these in the dataset finder brings you back here.
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+ 9 more — browse all 9 samples with per-sample file links →
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- GSE324432 A novel sorting method uncovers metabolic heterogeneity between mononucleated and binucleated tetraploid hepatocytes 15 samples
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- GSE314817 Multi-tissue, multi-time-point transcriptomic atlas of aging in mice and rats [mouse] 2432 samples
- GSE293709 Transcriptome analysis in the prefrontal cortex of different ASD mouse models treated with drug 1565 samples
- GSE294832 Modular neuroinflammatory network discovery from large-scale phenotypic screening in genetically heterogeneous mice [part10] 1000 samples
- GSE326100 scRNA-seq of mouse cochlea organoid cells 768 samples
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