Genetic basis of hereditary hypophosphataemic rickets and phenotype presentation in children and adults

by Tavana, Nahid, Thilakavathy, Karuppiah, Kennerson, Marina L., Ting, Tzer Hwu
Published 2021

Mutation analysis of SOD1, C9orf72, TARDBP and FUS genes in ethnically-diverse Malaysian patients with amyotrophic lateral sclerosis (ALS)

by Edgar, Suzanna, Ellis, Melina, Abdul-Aziz, Nur Adilah, Goh, Khean-Jin, Shahrizaila, Nortina, Kennerson, Marina L., Ahmad-Annuar, Azlina
Published 2021

Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family

by Tey, 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, Azlina
Published 2019