Correction: exome sequencing reveals novel and recurrent mutations with clinical significance in inherited retinal dystrophies.

Correction: exome sequencing reveals novel and recurrent mutations with clinical significance in inherited retinal dystrophies.

Bibliographic Details
Main Author: PLOS ONE Staff
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4361588?pdf=render

Internet

http://europepmc.org/articles/PMC4361588?pdf=render

Similar Items