Concepedia

Publication | Closed Access

Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia

DOI

127

Citations

14

References

2012

Year

M. Zimoń, Jonathan Baets, Leonardo Almeida‐Souza, Els De Vriendt, J. Nikodinović, Yeşim Parman, Esra Battaloğlu, Zeliha Matur, Velina Guergueltcheva, Ivailo Tournev,
Nature Genetics

References

YearCitations

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