 | Up a level |
Edgar, Suzanna and Ellis, Melina and Abdul-Aziz, Nur Adilah and Goh, Khean-Jin and Shahrizaila, Nortina and Kennerson, Marina L. and Ahmad-Annuar, Azlina (2021) Mutation analysis of SOD1, C9orf72, TARDBP and FUS genes in ethnically-diverse Malaysian patients with amyotrophic lateral sclerosis (ALS). Neurobiology of Aging, 108. pp. 200-206. ISSN 0197-4580, DOI https://doi.org/10.1016/j.neurobiolaging.2021.07.008.
Tey, Shelisa and Shahrizaila, Nortina and Drew, Alexander P. and Samulong, Sarimah and Goh, Khean Jin and Battaloglu, Esra and Atkinson, Derek and Parman, Yesim and Jordanova, Albena and Chung, Ki Wha and Choi, Byung-Ok and Li, Yi-Chung and Auer-Grumbach, Michaela and Nicholson, Garth A. and Kennerson, Marina L. and Ahmad-Annuar, Azlina (2019) Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family. Neurogenetics, 20 (3). pp. 117-127. ISSN 1364-6745, DOI https://doi.org/10.1007/s10048-019-00576-3.
