Table 1

Baseline characteristics for the study population

NoMale/female (no) (%)Age (years) at onset (range)Spinal/bulbar (no) (%)Mutations (no)Mutation frequency (%)
Sporadic amyotrophic lateral sclerosis451265/186 (59/41)59 (20 to 84)349/102 (77/23)20.44
Familial disposition for amyotrophic lateral sclerosis5529/26 (52/48)57 (24 to 80)51/4 (93/7)11.82
  • Survival is defined as the interval between age at onset and age of death or tracheostomy shown in months, with the range shown in parentheses.