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Genotypic and phenotypic spectrum of the most common causative genes of Charcot-Marie-Tooth disease in Hungarian patients.
Neuromuscul Disord. 2018 Jan;28(1):38-43. doi: 10.1016/j.nmd.2017.08.007. Epub 2017 Sep 8.
Neuromuscul Disord. 2018.
PMID: 29174527
Three novel mutations and genetic epidemiology analysis of the Gap Junction Beta 1 (GJB1) gene among Hungarian Charcot-Marie-Tooth disease patients.
Milley GM, Varga ET, Grosz Z, Bereznai B, Aranyi Z, Boczan J, Dioszeghy P, Kálmán B, Gal A, Molnar MJ.
Milley GM, et al.
Neuromuscul Disord. 2016 Oct;26(10):706-711. doi: 10.1016/j.nmd.2016.07.012. Epub 2016 Jul 27.
Neuromuscul Disord. 2016.
PMID: 27544631
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Asian-specific mitochondrial genome polymorphism (9-bp deletion) in Hungarian patients with mitochondrial disease.
Pentelenyi K, Remenyi V, Gal A, Milley GM, Csosz A, Mende BG, Molnar MJ.
Pentelenyi K, et al. Among authors: milley gm.
Mitochondrial DNA A DNA Mapp Seq Anal. 2016 May;27(3):1697-700. doi: 10.3109/19401736.2014.961128. Epub 2014 Sep 22.
Mitochondrial DNA A DNA Mapp Seq Anal. 2016.
PMID: 25242187
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Analysis of GJB2 mutations and the clinical manifestation in a large Hungarian cohort.
Kecskeméti N, Szönyi M, Gáborján A, Küstel M, Milley GM, Süveges A, Illés A, Kékesi A, Tamás L, Molnár MJ, Szirmai Á, Gál A.
Kecskeméti N, et al. Among authors: milley gm.
Eur Arch Otorhinolaryngol. 2018 Oct;275(10):2441-2448. doi: 10.1007/s00405-018-5083-4. Epub 2018 Aug 9.
Eur Arch Otorhinolaryngol. 2018.
PMID: 30094485
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