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Table 1 Summary of all cases used in this study. See supplementary data for subgroup analyses

From: Quantitative patterns of motor cortex proteinopathy across ALS genotypes

Genotype

n =

With FTD

Sex

Age (Years)

PMD (Hours)

Fixation (Weeks)

M

F

Range

Mean

Std. Dev.

Range

Mean

Std. Dev.

Range

Mean

Std. Dev.

Control

17

0

10

7

36–95

62.5

14.0

18–73

42.5

16.0

0.2–32

7.1

9.2

Sporadic

39

7

21

18

44–90

65.5

11.7

24–120

47.7

22.5

0.2–28

5.9

8.5

C9ORF72a

18

5

11

7

42–76

60.6

9.4

4–96

47.5

30.5

0.2–17

7.5

4.8

SOD1b

11

0

3

8

34–78

55.9

14.7

5–96

39.0

31.9

3–20

11.8

5.8

FUSc

9

0

4

5

18–64

37.9

15.2

19–72

47.0

19.5

2–45

12.6

13.7

CHMP2Bd

2

0

1

1

51–69

60.0

12.7

12–22

17.0

7.1

3–4.5

3.8

1.1

HNRNPA1e

1

0

0

1

62

62.0

–

48

48.0

–

12.0

12.0

–

OPTNf

1

0

1

0

54

54.0

–

72

72.0

–

12.0

12.0

–

TARDBPg

1

0

1

0

57

57.0

–

48

48.0

–

9.0

9.0

–

  1. aC9ORF72 – Chromosome 9 open reading frame 72; bSOD1 – Superoxide dismutase 1; cFUS – Fused-in-sarcoma; dCHMP2B – Charged multivesicular body protein 2B; eHNRNPA1 – Heterogeneous nuclear ribonucleoprotein A1; fOPTN – Optineurin; gTARDBP – TAR DNA-binding protein. PMD = post-mortem delay