SPTAN1 variants as a potential cause for autosomal recessive hereditary spastic paraplegia
Leveille, Etienne, Estiar, Mehrdad A., Krohn, Lynne, Spiegelman, Dan, Dionne-Laporte, Alexandre, Dupré, Nicolas, Trempe, Jean François, Rouleau, Guy A., Gan-Or, ZivLanguage:
english
Journal:
Journal of Human Genetics
DOI:
10.1038/s10038-019-0669-2
Date:
September, 2019
File:
PDF, 590 KB
english, 2019