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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
✍ Scribed by Xuan Huang; Mengnan Tian; Ciria C. Hernandez; Ningning Hu; Robert L. Macdonald
- Book ID
- 113812672
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 877 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0969-9961
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