APA

Laššuthová P., Brožková D. Š., Krůtová M., Neupauerová J., Haberlová J., Mazanec R., Dvořáčková N., Goldenberg Z. & Seeman P. (20150827). Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom. : Neurogenetics.

Chicago

Laššuthová P, Brožková D Šafka, Krůtová M, Neupauerová J, Haberlová J, Mazanec R, Dvořáčková N, Goldenberg Z and Seeman P. 20150827. Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom. : Neurogenetics.

Harvard

Laššuthová P., Brožková D. Š., Krůtová M., Neupauerová J., Haberlová J., Mazanec R., Dvořáčková N., Goldenberg Z. and Seeman P. (20150827). Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom. : Neurogenetics.

MLA

Laššuthová P, Brožková D Šafka, Krůtová M, Neupauerová J, Haberlová J, Mazanec R, Dvořáčková N, Goldenberg Z and Seeman P. Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom. : Neurogenetics. 20150827.