Associated Papers
MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia.
Selçuk E et al.
Molecular Genetics and Genomics : Mgg, 2022
XomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.
Talukder AK et al.
Plos One, 2015
25905921 (PubMed )
Supplement: pone.0123569.s008.xls › BC7_ERR166315
Role of spastin and protrudin in neurite outgrowth.
Zhang C et al.
Journal of Cellular Biochemistry, 2012
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