Results
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31241.
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31242.
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31255.
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31256.
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SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes. [electronic resource] by
- Fertleman, Caroline R
- Baker, Mark D
- Parker, Keith A
- Moffatt, Sarah
- Elmslie, Frances V
- Abrahamsen, Bjarke
- Ostman, Johan
- Klugbauer, Norbert
- Wood, John N
- Gardiner, R Mark
- Rees, Michele
Producer: 20070110
In:
Neuron vol. 52
Availability: No items available.
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31257.
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