New Case of Spinocerebellar Ataxia, Autosomal Recessive 4, Due to VPS13D Variants
Article in International Journal of Molecular Sciences (May 2024)
The most recent citing publications are shown below. View all 108 publications that cite this research output on Dimensions.
Autosomal recessive spinocerebellar ataxia type 4 due to a novel homozygous mutation in the VPS13D gene in a Saudi family
Article in Clinical Neurology and Neurosurgery (March 2024)
ER-organelle contacts: A signaling hub for neurological diseases
Article in Pharmacological Research (March 2024)