Associated Papers
Clinical characteristics and mutation spectrum in 33 Chinese families with familial exudative vitreoretinopathy.
Mao J et al.
Annals of Medicine, 2022
Pathogenic variants and associated phenotypic spectrum of TSPAN12 based on data from a large cohort.
Sun W et al.
Graefe's Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie, 2021
An Ophthalmic Targeted Exome Sequencing Panel as a Powerful Tool to Identify Causative Mutations in Patients Suspected of Hereditary Eye Diseases.
Wang P et al.
Translational Vision Science & Technology, 2019
31106028 (PubMed )
Supplement: tvst-08-02-12_s02.xlsx › FINAL-AD-AR-XL-ONE
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