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. 2020 May 18;16(5):e1007871. doi: 10.1371/journal.pcbi.1007871

Table 4. COS for patients with homozygous mutations.

Patient* Mutation Seizures Cognitive Disorders Brain malformations Muscle/
Movement Control
COS
5 I372F 3 - 3 3 9
8 C291Y 1 1 - - 2
17 R362C 1 1 - - 2
44 A389V - 1 - 2 3
45 A389V 1 2 - 2 5
46 A802V 0 0 - 2 2
47 A802V 0 0 - 0 0
48 A802V 0 0 - 0 0
49 A802V 0 1 - 2 3
50 R739H 1 1 - 2 4
53 Y623H 1 1 - 1 3
58 Y164H 1 2 0 2 5
59 Y164H 1 2 - 1 4
60 Y164H 1 1 - 0 2
62 Y161C 3 3 3 3 12
63 R988Q 1 - 3 3 7
72 P949L 3 3 3 - 9
75 P581R 1 3 3 - 7
77 A202V 1 1 - - 2
78 H950R 3 3 3 - 9
79 Q366R 1 2 - - 3
81 R515S 3 3 3 - 9
83 T269M 1 1 - - 2
130 D198V 3 - 3 3 9

*Number assigned on basis of S4A Table