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Autosomal Recessive Axonal Neuropathy With Neuromyotonia: A Rare Entity
Download from www.researchgate.netDeficiency of the E3 ubiquitin ligase TRIM2 in early-onset axonal neuropathy
Download from academic.oup.comLoss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia
Download from www.nature.comGenetic spectrum of hereditary neuropathies with onset in the first year of life
Download from doi.orgDominant GDAP1 mutations cause predominantly mild CMT phenotypes
Download from www.ncbi.nlm.nih.govReduced penetrance in hereditary motor neuropathy caused by **TRPV4** Arg269Cys mutation
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