Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleLinkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family.AuthorsTey, Shelisa; Shahrizaila, Nortina; Drew, Alexander P.; Samulong, Sarimah; Goh, Khean-Jin; Battaloglu, Esra; Atkinson, Derek; Parman, Yesim; Jordanova, Albena; Chung, Ki Wha; Choi, Byung-Ok; Li, Yi-Chung; Auer-Grumbach, Michaela; Nicholson, Garth A.; Kennerson, Marina L.; Ahmad-Annuar, AzlinaPublicationNeurogenetics, 2019, Vol 20, Issue 3, p117ISSN1364-6745Publication typeArticleDOI10.1007/s10048-019-00576-3