학술논문
The combination of whole-exome sequencing and clinical analysis allows better diagnosis of rare syndromic retinal dystrophies
Document Type
Article
Author
Source
In: Acta Ophthalmologica . (Acta Ophthalmologica, 2019, 97(6):e877-e886)
Subject
Language
English
ISSN
17553768
1755375X
1755375X