Associated Papers
Identification of Possible Risk Variants of Familial Strabismus Using Exome Sequencing Analysis.
An JY et al.
Genes, 2021
Whole Exome Sequencing in Eight Thai Patients With Leber Congenital Amaurosis Reveals Mutations in the CTNNA1 and CYP4V2 Genes.
Jinda W et al.
Investigative Ophthalmology & Visual Science, 2017
Select a paper to view details