Autofluorescence in female carriers with choroideremia: A familial case with a novel mutation in the CHM gene
Ortiz-Ramirez, Grecia Yael, Villanueva-Mendoza, Cristina, Zenteno Ruiz, Juan Carlos, Reyes, Mariana, Cortés-González, VianneyJournal:
Ophthalmic Genetics
DOI:
10.1080/13816810.2020.1810283
Date:
August, 2020
File:
PDF, 2.47 MB
2020