Fertleman CR et al. (2006). SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes. Neuron. 52 [PubMed]
See more from authors:
Fertleman CR
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Baker MD
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Parker KA
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Moffatt S
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Elmslie FV
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Abrahamsen B
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Ostman J
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Klugbauer N
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Wood JN
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Gardiner RM
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Rees M
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