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. 2012 Nov 6;79(19):1983–1989. doi: 10.1212/WNL.0b013e3182735d36

Table 2.

Main clinical characteristics of patients with different mutations and without known mutations

graphic file with name znl04312-0516-t02.jpg

Abbreviations: fALS = familial amyotrophic lateral sclerosis; FTD = frontotemporal dementia; IQR = interquartile range; NS = not significant; sALS = sporadic amyotrophic lateral sclerosis.

a

Calculated on 475 cases.

b

The 2 cases with FUS and OPTN missense mutations are not indicated in the table; both patients had a spinal phenotype and were cognitively normal.