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Timmerman V, Nelis E, Van Hul W, et al. The peripheral myelin protein gene <i>PMP-22<\/i> is contained within the Charcot-Marie-Tooth disease type 1A duplication. Nat Genet 1: 171-175, 1992.","DOI":"10.1038\/ng0692-171"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Bjelica B, Peric S, Basta I, et al. Neuropathic pain in patients with Charcot-Marie-Tooth type 1A. Neurol Sci 41: 625-630, 2020.","DOI":"10.1007\/s10072-019-04142-5"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Braathen GJ. Genetic epidemiology of Charcot-Marie-Tooth disease. Acta Neurol Scand 126: 1-22, 2012.","DOI":"10.1111\/ane.12013"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Karadima G, Floroskufi P, Koutsis G, Vassilopoulos D, Panas M. Mutational analysis of <i>PMP22<\/i>, <i>GJB1<\/i> and <i>MPZ<\/i> in Greek Charcot-Marie-Tooth type 1 neuropathy patients. Clin Genet 80: 497-499, 2011.","DOI":"10.1111\/j.1399-0004.2011.01657.x"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Marques W Jr, Freitas MR, Nascimento OJ, et al. 17p duplicated Charcot-Marie-Tooth 1A: characteristics of a new population. J Neurol 252: 972-979, 2005.","DOI":"10.1007\/s00415-005-0797-9"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Abe A, Numakura C, Kijima K, et al. Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan. J Hum Genet 56: 364-368, 2011.","DOI":"10.1038\/jhg.2011.20"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Reilly MM, Shy ME. Diagnosis and new treatments in genetic neuropathies. J Neurol Neurosurg Psychiatry 80: 1304-1314, 2009.","DOI":"10.1136\/jnnp.2008.158295"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Braathen GJ, Sand JC, Lobato A, H\u00f8yer H, Russell MB. Genetic epidemiology of Charcot-Marie-Tooth in the general population. 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Pediatr Clin North Am 62: 767-786, 2015.","DOI":"10.1016\/j.pcl.2015.03.012"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Pazzaglia C, Vollono C, Ferraro D, et al. Mechanisms of neuropathic pain in patients with Charcot-Marie-Tooth 1 A: a laser-evoked potential study. Pain 149: 379-385, 2010.","DOI":"10.1016\/j.pain.2010.03.001"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Laur\u00e0 M, Hutton EJ, Blake J, et al. Pain and small fiber function in Charcot-Marie-Tooth disease type 1A. Muscle Nerve 50: 366-371, 2014.","DOI":"10.1002\/mus.24169"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Azevedo H, Pupe C, Pereira R, Nascimento OJM. Pain in Charcot-Marie-Tooth disease: an update. Arq Neuropsiquiatr 76: 273-276, 2018.","DOI":"10.1590\/0004-282x20180021"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Joo IS, Ki CS, Joo SY, Huh K, Kim JW. A novel point mutation in <i>PMP22<\/i> gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafness. Neuromuscul Disord 14: 325-328, 2004.","DOI":"10.1016\/j.nmd.2004.02.009"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Luigetti M, Zollino M, Conti G, Romano A, Sabatelli M. Inherited neuropathies and deafness caused by a <i>PMP22<\/i> point mutation: a case report and a review of the literature. Neurol Sci 34: 1705-1707, 2013.","DOI":"10.1007\/s10072-012-1277-5"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Verhagen WI, Huygen PL, Gabre\u00ebls-Festen AA, Engelhart M, van Mierlo PJ, van Engelen BG. Sensorineural hearing impairment in patients with <i>Pmp22<\/i> duplication, deletion, and frameshift mutations. Otol Neurotol 26: 405-414, 2005.","DOI":"10.1097\/01.mao.0000169769.93173.df"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19. Lerat J, Magdelaine C, Roux AF, et al. 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