期刊
NATURE REVIEWS NEUROLOGY
卷 10, 期 2, 页码 70-72出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/nrneurol.2013.270
关键词
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Genetic research in frontotemporal lobar degeneration (FTLD) is gaining momentum. Following the discovery of a repeat expansion in the gene C9 open reading frame 72 (C9orf72), three major genes and associated disease mechanisms and inclusion body pathologies have emerged, paving the way for personalized medicine in FTLD.
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