Exome sequencing identifies novel missense and deletion variants in
RTN4IP1
associated with optic atrophy, global developmental delay, epilepsy, ataxia, and choreoathetosis
Exome sequencing identifies novel missense and deletion variants in
RTN4IP1
associated with optic atrophy, global developmental delay, epilepsy, ataxia, and choreoathetosis
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now