Associated Papers
Analysis of early-onset glaucoma genes in primary congenital glaucoma patients residing in North India identifies an additional case with THBS1 Arg1034Cys.
Somarajan BI et al.
Ophthalmic Genetics, 2025
Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanisms.
Reis LM et al.
Progress in Retinal and Eye Research, 2024
Thrombospondin Mutations and Patients With Primary Congenital Glaucoma in a United States Population.
Boese EA et al.
Journal of Glaucoma, 2023
Thrombospondin 1 missense alleles induce extracellular matrix protein aggregation and TM dysfunction in congenital glaucoma.
Fu H et al.
The Journal of Clinical Investigation, 2022
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