Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom
| Image |  |
|---|---|
| Description | scientific article published on 24 October 2014 |
| Author/s |
author: Petra Laššuthová |
| Publication date | October 24, 2014 |
| Language | |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |