Palmio, J., Kärppä, M., Baumann, P., Penttilä, S., Moilanen, J., & Udd, B. (2016). Novel compound heterozygous mutation in SACS gene leads to a milder autosomal recessive spastic ataxia of Charlevoix‐Saguenay, ARSACS, in a Finnish family. Clin Case Rep.

Palmio, Johanna, Mikko Kärppä, Peter Baumann, Sini Penttilä, Jukka Moilanen, and Bjarne Udd. "Novel Compound Heterozygous Mutation in SACS Gene Leads to a Milder Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay, ARSACS, in a Finnish Family." Clin Case Rep 2016.

Palmio, Johanna, et al. "Novel Compound Heterozygous Mutation in SACS Gene Leads to a Milder Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay, ARSACS, in a Finnish Family." Clin Case Rep 2016.