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SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Alle... | ResearchHub
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SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes
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Authors
Caroline Fertleman
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Caroline Fertleman
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Caroline Fertleman
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Michele Rees
Published
December 1, 2006
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Journal
Neuron
Topics
Biology
Neuroscience
Chemistry
Medicine
Physiology
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DOI
10.1016/j.neuron.2006.10.006
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publisher-specific-oa
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Journal
Neuron
Topics
Biology
Neuroscience
Chemistry
Medicine
Physiology
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DOI
10.1016/j.neuron.2006.10.006
License
publisher-specific-oa
