Literature DB >> 24813348

Channelopathy: a novel mutation in the SCN9A gene causes insensitivity to pain and autonomic dysregulation.

F Bartholomew1, J Lazar, A Marqueling, C Lee-Messer, S Jaradeh, J M C Teng.   

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Year:  2014        PMID： 24813348     DOI： 10.1111/bjd.13096

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


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  3 in total

1.  A novel SCN9A splicing mutation in a compound heterozygous girl with congenital insensitivity to pain, hyposmia and hypogeusia.

Authors:  Margherita Marchi; Vincenzo Provitera; Maria Nolano; Marcello Romano; Simona Maccora; Ilaria D'Amato; Erika Salvi; Monique Gerrits; Lucio Santoro; Giuseppe Lauria
Journal:  J Peripher Nerv Syst       Date:  2018-07-23       Impact factor: 3.494

2.  Selective Targeting of Nav1.7 with Engineered Spider Venom-Based Peptides.

Authors:  Robert A Neff; Alan D Wickenden
Journal:  Channels (Austin)       Date:  2021-12       Impact factor: 2.581

3.  Rare mutations in ATL3, SPTLC2 and SCN9A explaining hereditary sensory neuropathy and congenital insensitivity to pain in a Brazilian cohort.

Authors:  Vivian Pedigone Cintra; Maike F Dohrn; Pedro José Tomaselli; Fernanda Barbosa Figueiredo; Sandra Elisabete Marques; Sarah Teixeira Camargos; Luiz Sergio Mageste Barbosa; Adriana P Rebelo; Lisa Abreu; Matt Danzi; Wilson Marques; Stephan Züchner
Journal:  J Neurol Sci       Date:  2021-05-18       Impact factor: 4.553
  3 in total

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