Publication | Open Access
SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes
745
Citations
29
References
2006
Year
Allelic VariantMolecular NeuroscienceGenetic DisorderGeneticsPathologyDisease Gene IdentificationMedicineScn9a MutationsVariant InterpretationNeurogenetics
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