author-photo

Aurore Tourville

University of Paris

4

Papers

29

Citations

Citation Trend

Filter By

Papers (2) Sort By

Journal Conference Others

Identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindness

2019 Ophthalmic Genetics
Show All
- Source
- Cite
- Save
Citations (1)
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F ‐mediated inherited retinal disorders

2019 Human Mutation
Show All
- Source
- Cite
- Save
Citations (12)