Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom
Crossref DOI link: https://doi.org/10.1007/s10048-014-0427-8
Published Online: 2014-10-24
Published Print: 2015-01
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Laššuthová, P.
Brožková, D. Šafka
Krůtová, M.
Neupauerová, J.
Haberlová, J.
Mazanec, R.
Dvořáčková, N.
Goldenberg, Z.
Seeman, P.
Text and Data Mining valid from 2014-10-24