Childhood glaucoma genes and phenotypes: Focus on FOXC1 mutations causing anterior segment dysgenesis and hearing loss
Year: 2019
Type: review
Source: Experimental Eye Research
Authors: Angela C. Gauthier, Janey L. Wiggs
Institutions: Massachusetts Eye and Ear Infirmary, Harvard University
Language: English
Subfield: Ophthalmology
Field: Medicine
Domain: Health Sciences
Open Access status: green
OpenAlex ID: W2996149878
