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Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese

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Academic year: 2020

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Figure

Table 1 Genes identified from analysis of rare variant counts in combined Chinese and European ancestry data
Fig. 1 QuantileLOF (Additional file 2: Figure S1). Test statistics are provided for the genes with the top ten associations (qualifying variants were observed in controls for genecorrected significance threshold was–quantile plots of the analysis of rare v
Fig. 2 Summary of rare variants in Chinese WES sample comprising 597 sporadic (sALS) and 13 familial (fALS) cases

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