PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema
Crossref DOI link: https://doi.org/10.1007/s12311-016-0784-y
Published Online: 2016-05-10
Published Print: 2017-02
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Tzoulis, C.
Sztromwasser, Paweł
Johansson, Stefan
Gjerde, Ivar Otto
Knappskog, Per
Bindoff, L. A.
Funding for this research was provided by:
Helse Vest Regionalt Helseføretak (911903, 911988, 911810)
License valid from 2016-05-10