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PubMed (OMIM) for id: 3094

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Page 1
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
Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.
Zimoń M, Baets J, Almeida-Souza L, De Vriendt E, Nikodinovic J, Parman Y, Battaloğlu E, Matur Z, Guergueltcheva V, Tournev I, Auer-Grumbach M, De Rijk P, Petersen BS, Müller T, Fransen E, Van Damme P, Löscher WN, Barišić N, Mitrovic Z, Previtali SC, Topaloğlu H, Bernert G, Beleza-Meireles A, Todorovic S, Savic-Pavicevic D, Ishpekova B, Lechner S, Peeters K, Ooms T, Hahn AF, Züchner S, Timmerman V, Van Dijck P, Rasic VM, Janecke AR, De Jonghe P, Jordanova A. Zimoń M, et al. Nat Genet. 2012 Oct;44(10):1080-3. doi: 10.1038/ng.2406. Epub 2012 Sep 9. Nat Genet. 2012. PMID: 22961002
[Neuromyotonia].
Mertens HG, Zschocke S. Mertens HG, et al. Klin Wochenschr. 1965 Sep 1;43(17):917-25. doi: 10.1007/BF01712058. Klin Wochenschr. 1965. PMID: 5863557 German. No abstract available.
Neuromyotonia in hereditary motor neuropathy.
Hahn AF, Parkes AW, Bolton CF, Stewart SA. Hahn AF, et al. J Neurol Neurosurg Psychiatry. 1991 Mar;54(3):230-5. doi: 10.1136/jnnp.54.3.230. J Neurol Neurosurg Psychiatry. 1991. PMID: 1851512 Free PMC article.