Matches in DBpedia 2015-10 for { ?s ?p "Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness" }
Showing triples 1 to 1 of
1
with 100 triples per page.
DBpedia – Linked Data Fragments
