Novel SCN9A mutations underlying extreme pain phenotypes: unexpected electrophysiological and clinical phenotype correlations.
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Nav1.7 and other voltage-gated sodium channels as drug targets for pain reliefPharmacological characterisation of the highly NaV1.7 selective spider venom peptide Pn3a.Advanced Genetic Testing Comes to the Pain Clinic to Make a Diagnosis of Paroxysmal Extreme Pain Disorder.Functional Studies of Sodium Channels: From Target to Compound Identification.[EXPRESS] Single Nucleotide Polymorphism in the COL11A2 Gene Associated with Heat Pain Sensitivity in Knee OsteoarthritisSodium channel slow inactivation interferes with open channel block.Advances in understanding nociception and neuropathic pain.
P2860
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P2860
Novel SCN9A mutations underlying extreme pain phenotypes: unexpected electrophysiological and clinical phenotype correlations.
description
2015 nî lūn-bûn
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年论文
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2015年论文
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2015年论文
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name
Novel SCN9A mutations underlyi ...... inical phenotype correlations.
@ast
Novel SCN9A mutations underlyi ...... inical phenotype correlations.
@en
type
label
Novel SCN9A mutations underlyi ...... inical phenotype correlations.
@ast
Novel SCN9A mutations underlyi ...... inical phenotype correlations.
@en
prefLabel
Novel SCN9A mutations underlyi ...... inical phenotype correlations.
@ast
Novel SCN9A mutations underlyi ...... inical phenotype correlations.
@en
P2093
P2860
P50
P1476
Novel SCN9A mutations underlyi ...... inical phenotype correlations.
@en
P2093
Adeline K Nicholas
C Geoffrey Woods
James J Cox
P2860
P304
P356
10.1523/JNEUROSCI.3935-14.2015
P407
P577
2015-05-01T00:00:00Z