Associated Papers
Genetic variants of TSPAN12 gene in patients with retinopathy of prematurity.
Zhang T et al.
Journal of Cellular Biochemistry, 2019
Familial Exudative Vitreoretinopathy-Related Disease-Causing Genes and Norrin/β-Catenin Signal Pathway: Structure, Function, and Mutation Spectrums.
Xiao H et al.
Journal of Ophthalmology, 2019
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.
Al Turki S et al.
American Journal of Human Genetics, 2016
Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy.
Poulter JA et al.
American Journal of Human Genetics, 2016
Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.
Poulter JA et al.
American Journal of Human Genetics, 2010
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