Investigating genotype–phenotype relationship of extreme neuropathic pain disorders in a UK national cohort

The aims of our study were to use whole genome sequencing in a cross-sectional cohort of patients to identify new variants in genes implicated in neuropathic pain, to determine the prevalence of known pathogenic variants and to understand the relationship between pathogenic variants and clinical pre...

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Detalles Bibliográficos
Autores principales: Themistocleous, Andreas C, Baskozos, Georgios, Blesneac, Iulia, Comini, Maddalena, Megy, Karyn, Chong, Sam, Deevi, Sri V V, Ginsberg, Lionel, Gosal, David, Hadden, Robert D M, Horvath, Rita, Mahdi-Rogers, Mohamed, Manzur, Adnan, Mapeta, Rutendo, Marshall, Andrew, Matthews, Emma, McCarthy, Mark I, Reilly, Mary M, Renton, Tara, Rice, Andrew S C, Vale, Tom A, van Zuydam, Natalie, Walker, Suellen M, Woods, Christopher Geoffrey, Bennett, David L H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9991512/
https://www.ncbi.nlm.nih.gov/pubmed/36895957
http://dx.doi.org/10.1093/braincomms/fcad037

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9991512/
https://www.ncbi.nlm.nih.gov/pubmed/36895957
http://dx.doi.org/10.1093/braincomms/fcad037

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