Cite
HARVARD Citation
Balint, B. et al. (2020). KCNN2 mutation in autosomal‐dominant tremulous myoclonus‐dystonia. European journal of neurology. pp. 1471-1477. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Balint, B. et al. (2020). KCNN2 mutation in autosomal‐dominant tremulous myoclonus‐dystonia. European journal of neurology. pp. 1471-1477. [Online].