Trudeau, M. M., Dalton, J. C., Day, J. W., Ranum, L. P. W., & Meisler, M. H. (2006). Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation. BMJ Group.

Trudeau, M M., J C. Dalton, J W. Day, L P W. Ranum, and M H. Meisler. Heterozygosity for a Protein Truncation Mutation of Sodium Channel SCN8A in a Patient With Cerebellar Atrophy, Ataxia, and Mental Retardation. BMJ Group, 2006.

Trudeau, M M., et al. Heterozygosity for a Protein Truncation Mutation of Sodium Channel SCN8A in a Patient With Cerebellar Atrophy, Ataxia, and Mental Retardation. BMJ Group, 2006.