QuickView for KIF1A (gene)

1. Insight into the regulation of axonal transport from the study of KIF1A-associated neurological diso…
2. Identification of an in-frame homozygous KIF1A variant causing a mild SPG30 phenotype in a Korean fa…
3. A de novo low-frequency mosaic variant of KIF1A causes hereditary spastic paraplegia: A literature r…
4. KIF1A gene-associated neurological disease: the correlation between genotype and phenotype].
5. Lattice light-sheet microscopy and evaluation of dendritic transport in cultured hippocampal tissue …

There were no clinical trials for KIF1A