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Mutation p.G83R in the transthyretin gene is associated with hereditary vitreous amyloidosis in Han Chinese families
PURPOSE: Hereditary vitreous amyloidosis (HVA) is a genetic ophthalmological disorder. The purpose of this study was to investigate whether a mutation in the transthyretin (TTR) gene is associated with HVA in Han Chinese families. METHODS: We performed clinical evaluation of three Han Chinese famili...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Molecular Vision
2013
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724954/ https://www.ncbi.nlm.nih.gov/pubmed/23901247 |