Case Report: Hereditary transthyretin (ATTRv) amyloidosis: The p.G103R mutation of the transthyretin gene in a Han Chinese family is associated with vitreous hemorrhage.

Shen, Junhui; Yu, Hao; Lin, Jijian; Zhang, Li; Pan, Xiaohong; Chen, Zhiqing

Shen, Junhui; Yu, Hao; Lin, Jijian; Zhang, Li; Pan, Xiaohong; Chen, Zhiqing.

Afiliación

Shen J; Eye Center, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yu H; Department of Neurology and Department of Medical Genetics in Second Affiliated Hospital, and Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, Hangzhou, China.
Lin J; Eye Center, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Zhang L; Eye Center, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Pan X; Department of Cardiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Chen Z; Eye Center, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Front Genet ; 13: 972501, 2022.

Article en En | MEDLINE | ID: mdl-36186469

Palabras clave

hereditary transthyretin (ATTRv) amyloidosis; mutation; transthyretin gene; vitreous hemorrhage; vitreous opacity

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Genet Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

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