Intra- and interfamily phenotypic diversity in pain syndromes associated with a gain-of-function variant of NaV1.7.

scientific article published on 2 December 2011

Intra- and interfamily phenotypic diversity in pain syndromes associated with a gain-of-function variant of NaV1.7. is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1012215026
P356DOI10.1186/1744-8069-7-92
P932PMC publication ID3248882
P698PubMed publication ID22136189
P5875ResearchGate publication ID51848433

P50authorGiuseppe LauriaQ47739372
Catharina G FaberQ57051259
Mark EstacionQ73893911
Sulayman D Dib-HajjQ85290384
Stephen G WaxmanQ91085251
Ingemar S J MerkiesQ130279190
Janneke G. J. HoeijmakersQ130292565
Chongyang HanQ130292895
Monique M. GerritsQ130292940
Jin-Sung ChoiQ40526890
P2093author name stringJoost P H Drenth
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Can robots patch-clamp as well as humans? Characterization of a novel sodium channel mutationQ44180217
NaV1.7 gain-of-function mutations as a continuum: A1632E displays physiological changes associated with erythromelalgia and paroxysmal extreme pain disorder mutations and produces symptoms of both disorders.Q46301976
P304page(s)92
P577publication date2011-12-02
P1433published inMolecular PainQ15766244
P1476titleIntra- and interfamily phenotypic diversity in pain syndromes associated with a gain-of-function variant of NaV1.7.
P478volume7

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