A novel disorder reveals clathrin heavy chain-22 is essential for human pain and touch development

Congenital inability to feel pain is very rare but the identification of causative genes has yielded significant insights into pain pathways and also novel targets for pain treatment. We report a novel recessive disorder characterized by congenital insensitivity to pain, inability to feel touch, and...

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Detalles Bibliográficos
Autores principales: Nahorski, Michael S., Al-Gazali, Lihadh, Hertecant, Jozef, Owen, David J., Borner, Georg H. H., Chen, Ya-Chun, Benn, Caroline L., Carvalho, Ofélia P., Shaikh, Samiha S., Phelan, Anne, Robinson, Margaret S., Royle, Stephen J., Woods, C. Geoffrey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511860/
https://www.ncbi.nlm.nih.gov/pubmed/26068709
http://dx.doi.org/10.1093/brain/awv149

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511860/
https://www.ncbi.nlm.nih.gov/pubmed/26068709
http://dx.doi.org/10.1093/brain/awv149

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