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...

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Detalles Bibliográficos
Autores principales: Zhang, A-Mei, Wang, Hui, Sun, Peng, Hu, Qiu-Xiang, He, Yuqing, Yao, Yong-Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724954/
https://www.ncbi.nlm.nih.gov/pubmed/23901247

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724954/
https://www.ncbi.nlm.nih.gov/pubmed/23901247

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