
Axonal Neuropathy with Neuromyotonia
References
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- Zimoń M Baets J Almeida-Souza L De Vriendt E Nikodinovic J Parman Y Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia Nat Genet 2012 Oct 44 10 1080 3 10.1038/ng.2406 22961002
DOI: https://doi.org/10.15844/pedneurbriefs-28-2-5 | Journal eISSN: 2166-6482
Language: English
Page range: 12 - 12
Published on: Feb 1, 2014
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
Keywords:
© 2014 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.