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. Author manuscript; available in PMC: 2018 Jul 1.
Published in final edited form as: J Neurol. 2016 Nov 25;264(7):1320–1333. doi: 10.1007/s00415-016-8350-6

Table 1.

Numbers of studies and scans for each genetic disorder included in systematic review

Gene Number of studies Total number of scans Percentage of studies Percentage of scans
ACTA1 1 4 1.1 0.2
COL6 5 58 5.7 3.0
DES 1 4 1.1 0.2
DMPK 7 99 8.0 5.2
CNBP 3 23 3.4 1.2
DMD 23 689 26.4 35.9
Duchenne 16 554 18.4 28.9
Becker 6 123 6.9 6.4
Carrier 1 12 1.1 0.6
FSHD 14 617 16.1 32.2
CAPN 3 22 3.4 1.1
DYSF 6 143 6.9 7.5
FKRP 3 51 3.4 2.7
ANO5 2 30 2.3 1.6
LMNA 4 38 4.6 2.0
MATR3 1 16 1.1 0.8
MYOT 2 13 2.3 0.7
NEB 1 6 1.1 0.3
PABN 2 18 2.3 0.9
RYR1 2 15 2.3 0.8
SEPN1 2 13 2.3 0.7
TTN 1 22 1.1 1.1
TPM2 2 12 2.3 0.6
TIA1 1 11 1.1 0.6
MYH7 1 14 1.1 0.7
Total 87 1918 100.0 100.0