Severe retinal degeneration at an early age in Usher syndrome type 1B associated with homozygous splice site mutations in MYO7A gene
Abdelkader, Ehab, Enani, Lama, Schatz, Patrik, Safieh, LeenLanguage:
english
Journal:
Saudi Journal of Ophthalmology
DOI:
10.1016/j.sjopt.2017.10.004
Date:
October, 2017
File:
PDF, 1.88 MB
english, 2017