DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
LinksClose Window
References
Sawal HA, Harripaul R, Mikhailov A. et al.
Biallelic truncating SCN9A mutation identified in four families with congenital insensitivity to pain from Pakistan.
Clin Genet 2016;
90 (06) 563-565
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.