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Table 1 Types of novel variations detected in patients with congenital stationary night blindness in this study

From: Clinical and genetic studies for a cohort of patients with congenital stationary night blindness

Gene

Missense

Nonsense

Frameshift

Deletion

Splicing

Total

NYX

3

2

0

2

0

7

CACNA1F

4

2

1

1

1

9

TRPM1

9

1

0

3

1

14

GRM6

2

0

0

0

0

2