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Correlation between Weakness and Axonal Loss in Patients with CMT1A.
Krajewski K, Turansky C, Lewis R, Garbern J, Hinderer S, Kamholz J, Shy ME. Krajewski K, et al. Ann N Y Acad Sci. 1999 Oct;883(1):490-492. doi: 10.1111/j.1749-6632.1999.tb08618.x. Ann N Y Acad Sci. 1999. PMID: 29086958 No abstract available.
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2.
Züchner S, De Jonghe P, Jordanova A, Claeys KG, Guergueltcheva V, Cherninkova S, Hamilton SR, Van Stavern G, Krajewski KM, Stajich J, Tournev I, Verhoeven K, Langerhorst CT, de Visser M, Baas F, Bird T, Timmerman V, Shy M, Vance JM. Züchner S, et al. Among authors: krajewski km. Ann Neurol. 2006 Feb;59(2):276-81. doi: 10.1002/ana.20797. Ann Neurol. 2006. PMID: 16437557
CMT1X phenotypes represent loss of GJB1 gene function.
Shy ME, Siskind C, Swan ER, Krajewski KM, Doherty T, Fuerst DR, Ainsworth PJ, Lewis RA, Scherer SS, Hahn AF. Shy ME, et al. Among authors: krajewski km. Neurology. 2007 Mar 13;68(11):849-55. doi: 10.1212/01.wnl.0000256709.08271.4d. Neurology. 2007. PMID: 17353473
307 results