tallózása szerző szerint "Milley, György"

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Asian-specific mitochondrial genome polymorphism (9-bp deletion) in Hungarian patients with mitochondrial disease

Pentelényi, Klára; Reményi, Viktória; Gál, Anikó; Milley, György; Csosz A; Mende, Balázs Gusztáv; Molnár, Mária Judit (2016)

A 9-bp deletion of the mtDNA is known as an anthropological marker of people with East-Asian origin. This 9-bp mtDNA deletion was analyzed in 1073 Hungarians with suspected mitochondrial disease and in 468 healthy control ...
Three novel mutations and genetic epidemiology analysis of the Gap Junction Beta 1 (GJB1) gene among Hungarian Charcot-Marie-Tooth disease patients.

Milley, György; Varga, Edina Tímea; Grosz, Zoltán; Bereznai, Benjamin; Arányi, Zuzsanna; Boczan, J; Dioszeghy, P; Kalman, B; Gál, Anikó; Molnár, Mária Judit (2016)

Pathogenic variants of the gap junction beta 1 (GJB1) gene are responsible for the Charcot-Marie-Tooth neuropathy X type 1 (CMTX1). In this study, we report the mutation frequency of GJB1 in 210 Hungarian CMT patients and ...

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