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Year | Number of Results |
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2012 | 1 |
2021 | 1 |
2024 | 0 |
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Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.
Nat Genet. 2012 Oct;44(10):1080-3. doi: 10.1038/ng.2406. Epub 2012 Sep 9.
Nat Genet. 2012.
PMID: 22961002
HINT1-related neuropathy in Greek patients with Charcot-Marie-Tooth disease.
Kontogeorgiou Z, Voudommatis C, Kartanou C, Pandis D, Breza M, Zambelis T, Stefanis L, Panas M, Koutsis G, Karadima G.
Kontogeorgiou Z, et al.
J Peripher Nerv Syst. 2021 Dec;26(4):444-448. doi: 10.1111/jns.12473. Epub 2021 Oct 29.
J Peripher Nerv Syst. 2021.
PMID: 34694653
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