Associated Papers
A novel nonsense mutation in SCN9A in a Moroccan child with congenital insensitivity to pain.
Mansouri M et al.
Pediatric Neurology, 2014
Two novel SCN9A gene heterozygous mutations may cause partial deletion of pain perception.
Yuan R et al.
Pain Medicine (malden, Mass.), 2011
Two novel mutations of SCN9A (Nav1.7) are associated with partial congenital insensitivity to pain.
Staud R et al.
European Journal of Pain (london, England), 2011
A novel mutation in the SCN9A gene associated with congenital insensitivity to pain, anhidrosis, and mild cognitive impairment.
Romagnuolo M et al.
Pediatric Dermatology, 0
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