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A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia
Rydning, Siri Lynne, Dudesek, Ales, Rimmele, Florian, Funke, Claudia, Krüger, Stefanie, Biskup, Saskia, Vigeland, Magnus D., Hjorthaug, Hanne S., Sejersted, Yngve, Tallaksen, Chantal, Selmer, Kaja K.,Language:
english
Journal:
European Journal of Neurology
DOI:
10.1111/ene.13625
Date:
March, 2018
File:
PDF, 358 KB
english, 2018