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Identification of Novel Copy Number Variations of VCAN Gene in Three Chinese Families with Wagner Disease
The VCAN/versican gene encodes an important component of the extracellular matrix, the chondroitin sulfate proteoglycan 2 (CSPG2/versican). Heterozygous variants targeting exon 8 of VCAN have been shown to cause Wagner disease, a rare autosomal dominant non-syndromic vitreoretinopathy that induces r...
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| Publicado no: | Genes (Basel) |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7564609/ https://ncbi.nlm.nih.gov/pubmed/32854301 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes11090992 |
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