The phenotype of congenital insensitivity to pain due to the Na(V)1.9 variant p.L811P

Por Woods, Christopher Geoffrey, Babiker, Mohamed Osman Eltahir, Horrocks, Iain, Tolmie, John, Kurth, Ingo
Publicado no Eur J Hum Genet (2015)

The phenotype of congenital insensitivity to pain due to the Na(V)1.9 variant p.L811P

Por Woods, Christopher Geoffrey, Babiker, Mohamed Osman Eltahir, Horrocks, Iain, Tolmie, John, Kurth, Ingo
Publicado no Eur J Hum Genet (2015)

A Comprehensive Functional Analysis of NTRK1 Missense Mutations Causing Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN IV)

Por Shaikh, Samiha S., Chen, Ya‐Chun, Halsall, Sally‐Anne, Nahorski, Michael S., Omoto, Kiyoyuki, Young, Gareth T., Phelan, Anne, Woods, Christopher Geoffrey
Publicado no Hum Mutat (2016)