Associated Papers
Detailed structural abnormalities associated with a novel VCAN variant in a family with versican vitreoretinopathy.
Zhong A et al.
Ophthalmic Genetics, 2025
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family.
Bigoni S et al.
Frontiers in Genetics, 2018
A family with Wagner syndrome with uveitis and a new versican mutation.
Rothschild PR et al.
Molecular Vision, 2013
A new VCAN/versican splice acceptor site mutation in a French Wagner family associated with vascular and inflammatory ocular features.
Brézin AP et al.
Molecular Vision, 2011
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