HnRNPR strongly represses splicing of a critical exon associated with spinal muscular atrophy through binding to an exonic AU-rich element
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DOI: 10.1136/jmg-2023-109186
Abstract: Background Spinal muscular atrophy (SMA) is a motor neuron disease caused by mutations of survival of motor neuron 1 (SMN1) gene, which encodes the SMN protein. SMN2, a nearly identical copy of SMN1, with several… read more here.
Keywords: spinal muscular; muscular atrophy; rich element; hnrnpr ... See more keywords