Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness
| Image |  |
|---|---|
| Description | scientific article |
| Author/s |
author: Susanne Kohl Marie-Elise Lancelot Elise Orhan Mélanie Letexier Aline Antonio Christelle Michiels Béatrice Bocquet Claire Audier Samuel G. Jacobson Isabelle Audo Florian Sennlaub Marion Neuillé José-Alain Sahel Kinga Bujakowska Christina Zeitz Odile Lecompte |
| Publication date | December 13, 2012 |
| Language | English |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |