Cite
HARVARD Citation
Anand, G. et al. (n.d.). Autosomal dominant SCN8A mutation with an unusually mild phenotype. European journal of paediatric neurology. pp. 761-765. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Anand, G. et al. (n.d.). Autosomal dominant SCN8A mutation with an unusually mild phenotype. European journal of paediatric neurology. pp. 761-765. [Online].