Potter Heather D

SVEP1 as a Genetic Modifier of TEK-Related Primary Congenital Glaucoma.

We provide further evidence for PCG caused by TEK haploinsufficiency, affirm autosomal dominant inheritance in two pedigrees, and propose SVEP1 as a modifier of TEK expression during SC development, affecting disease penetrance and severity.

Scleritis with Devastating Consequences.