Associated Papers
A novel splicing variant of VCAN identified in a Chinese family initially diagnosed with familial exudative vitreoretinopathy.
Zhong J et al.
Molecular Genetics & Genomic Medicine, 2023
Clinical and genetic study on two Chinese families with Wagner vitreoretinopathy.
Li H et al.
Ophthalmic Genetics, 2020
Identification of Novel Copy Number Variations of VCAN Gene in Three Chinese Families with Wagner Disease.
Li S et al.
Genes, 2020
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family.
Bigoni S et al.
Frontiers in Genetics, 2018
Congenital glaucoma in Wagner syndrome.
Jewsbury H et al.
Journal of Aapos : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus, 2014
Novel VCAN mutations and evidence for unbalanced alternative splicing in the pathogenesis of Wagner syndrome.
Kloeckener-Gruissem B et al.
European Journal of Human Genetics : Ejhg, 2013
A family with Wagner syndrome with uveitis and a new versican mutation.
Rothschild PR et al.
Molecular Vision, 2013
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