We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA nullimorphic ERLIN2 mutation defines a complicated hereditary spastic paraplegia locus (SPG18).AuthorsAlazami, Anas; Adly, Nouran; Al Dhalaan, Hisham; Alkuraya, FowzanPublicationNeurogenetics, 2011, Vol 12, Issue 4, p333ISSN1364-6745Publication typearticleDOI10.1007/s10048-011-0291-8