Network topology of NaV1.7 mutations in sodium channel-related painful disorders

BACKGROUND: Gain-of-function mutations in SCN9A gene that encodes the voltage-gated sodium channel NaV1.7 have been associated with a wide spectrum of painful syndromes in humans including inherited erythromelalgia, paroxysmal extreme pain disorder and small fibre neuropathy. These mutations change...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:BMC Syst Biol
Autors principals: Kapetis, Dimos, Sassone, Jenny, Yang, Yang, Galbardi, Barbara, Xenakis, Markos N., Westra, Ronald L., Szklarczyk, Radek, Lindsey, Patrick, Faber, Catharina G., Gerrits, Monique, Merkies, Ingemar S. J., Dib-Hajj, Sulayman D., Mantegazza, Massimo, Waxman, Stephen G., Lauria, Giuseppe
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2017
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5324268/
https://ncbi.nlm.nih.gov/pubmed/28235406
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12918-016-0382-0
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars