期刊
NATURE REVIEWS NEUROLOGY
卷 9, 期 5, 页码 241-242出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/nrneurol.2013.72
关键词
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Genetic diagnosis of frontotemporal lobar degeneration has become challenging since the identification of a number of autosomal dominantly inherited causative mutations. As highlighted in a new paper, careful characterization of the clinical picture associated with a specific gene defect is mandatory to guide genetic screening, and to establish a diagnostic algorithm for neurology practice.
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