Tzoulis, C., Johansson, S., Haukanes, B. I., Boman, H., Knappskog, P. M., & Bindoff, L. A. (2013). Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay. Public Library of Science.
Citación estilo ChicagoTzoulis, Charalampos, Stefan Johansson, Bjørn Ivar Haukanes, Helge Boman, Per Morten Knappskog, y Laurence A. Bindoff. Novel SACS Mutations Identified By Whole Exome Sequencing in a Norwegian Family With Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay. Public Library of Science, 2013.
Cita MLATzoulis, Charalampos, et al. Novel SACS Mutations Identified By Whole Exome Sequencing in a Norwegian Family With Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay. Public Library of Science, 2013.