five

RNASeq_of_mouse_DDD_models_Phase_II

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NIAID Data Ecosystem2026-04-29 收录
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https://www.ncbi.nlm.nih.gov/sra/ERP023313
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Exome sequencing in children with developmental disorders has identified numerous causative mutations in novel disease genes. Using engineered loss of function alleles, we are modelling these disorders in mice. To understand the molecular and cellular mechanisms underpinning these neurodevelopmental disorders, we are carrying out RNA-sequencing of several distinct brain regions in adult animals, as well as brains from embryonic time points.
创建时间:
2021-02-04
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