The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1
Main Authors: | , , , , , , |
---|---|
格式: | Conference item |
语言: | English |
出版: |
Association for Research in Vision and Ophthalmology
2018
|
Main Authors: | , , , , , , |
---|---|
格式: | Conference item |
语言: | English |
出版: |
Association for Research in Vision and Ophthalmology
2018
|