An SCN9A channelopathy causes congenital inability to experience pain Cox et al. (2006) Nature 444: 894–898Loss‐of‐function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations Goldberg et al. (2007) Clin Genet 71: 311–319A stop codon mutation in SCN9A causes lack of pain sensation Ahmad et al. (2007) Hum Mol Genet 16: 2114–2121‘We cannot learn without pain.’– Aristotle
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