The GABRG2 nonsense mutation, Q40X, associated with Dravet syndrome activated NMD and generated a truncated subunit that was partially rescued by aminoglycoside-induced stop codon read-through
Xuan Huang, Mengnan Tian, Ciria C. Hernandez, Ningning Hu, Robert L. MacDonald
Research output: Contribution to journal › Article › peer-review
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