A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia.
Rydning SL1,2, Dudesek A3,4, Rimmele F3,4, Funke C5, Krüger S5, Biskup S5,6, Vigeland MD7, Hjorthaug HS7, Sejersted Y7, […]
Rydning SL1,2, Dudesek A3,4, Rimmele F3,4, Funke C5, Krüger S5, Biskup S5,6, Vigeland MD7, Hjorthaug HS7, Sejersted Y7, […]