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
Identification of Novel Copy Number Variations of VCAN Gene in Three Chinese Families with Wagner Disease.
Li S et al.
Genes, 2020
A family with Wagner syndrome with uveitis and a new versican mutation.
Rothschild PR et al.
Molecular Vision, 2013
Mutational hot spot potential of a novel base pair mutation of the CSPG2 gene in a family with Wagner syndrome.
Ronan SM et al.
Archives of Ophthalmology (chicago, Ill. : 1960), 2009
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