High-throughput sequencing revealed a novel SETX mutation in a Hungarian patient with amyotrophic lateral sclerosis

Kornélia Tripolszki, Dóra Török, David Goudenège, Katalin Farkas, Adrienn Sulák, Nóra Török, József I. Engelhardt, Péter Klivényi, Vincent Procaccio, Nikoletta Nagy, Márta Széll

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Medicine & Life Sciences