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Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivation
✍ Scribed by Lee, H.; Lin, M.-c. A.; Kornblum, H. I.; Papazian, D. M.; Nelson, S. F.
- Book ID
- 121659587
- Publisher
- Oxford University Press
- Year
- 2014
- Tongue
- English
- Weight
- 447 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0964-6906
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