We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleHeterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardationAuthorsTrudeau, M M; Dalton, J C; Day, J W; Ranum, L P W; Meisler, M HPublicationJournal of Medical Genetics (JMG), 2006, Vol 43, Issue 6, p527ISSN0022-2593Publication typearticle