PublicationsMutations in TRPM1 are a common cause of complete congenital stationary night blindness.
![Decorative header background](https://nin.nl/wp-content/themes/stuurlui/assets/img/header-bg-purple.png)
Support our work!
The Friends Foundation facilitates groundbreaking brain research. You can help us with that.
Support our workThe Friends Foundation facilitates groundbreaking brain research. You can help us with that.
Support our work