相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients
Annemarie Huebers et al.
NEUROBIOLOGY OF AGING (2015)
FUS-NLS/Transportin 1 Complex Structure Provides Insights into the Nuclear Targeting Mechanism of FUS and the Implications in ALS
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Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation
Ian R. A. Mackenzie et al.
ACTA NEUROPATHOLOGICA (2011)
SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis
Antonio Orlacchio et al.
BRAIN (2010)
SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotyp-phenotype correlations
Stephanie Millecamps et al.
JOURNAL OF MEDICAL GENETICS (2010)
Incidence of amyotrophic lateral sclerosis in Europe
Giancarlo Logroscino et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2010)
Natural history of young-adult amyotrophic lateral sclerosis
M. Sabatelli et al.
NEUROLOGY (2008)
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