Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleHomozygous mutation, p.Pro304His, in IDH3A, encoding isocitrate dehydrogenase subunit is associated with severe encephalopathy in infancy.AuthorsFattal-Valevski, Aviva; Eliyahu, Hila; Fraenkel, NItai; Elmaliach, Ganit; Hausman-Kedem, Moran; Shaag, Avraham; Mandel, Dror; Pines, Ophry; Elpeleg, OrlyPublicationNeurogenetics, 2017, Vol 18, Issue 1, p57ISSN1364-6745Publication typeArticleDOI10.1007/s10048-016-0507-z