ArticlePloS one2015
Correction: exome sequencing reveals novel and recurrent mutations with clinical significance in inherited retinal dystrophies.
PLOS ONE StaffPubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
ArticlePloS one2015
PLOS ONE StaffPubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.