Clinical and functional evidence for the pathogenicity of the <i>LRRK2</i> p.Arg1067Gln variant
New insights from a Malaysian real-world deep brain stimulation cohort
<i>ATXN2</i> polyglutamine intermediate repeats length expansions in Malaysian patients with amyotrophic lateral sclerosis (ALS)
Rare <i>SV2C</i> coding variants in Parkinson's disease risk
The Molecular Diagnosis of Myotonic Dystrophy in Malaysia.
Genetic mutations in sarcoglycanopathies in a Malaysian population.
