Clinical and biochemical characterization of hereditary transthyretin amyloidosis caused by E61K mutation

Objects: This study was intended to find out more about the clinical characterizations of patients carrying transthyretin (TTR) E61K (p.Glu81Lys) gene mutation and the biochemical characterization of this mutant protein. Materials and methods: Five patients who had been diagnosed with hereditary tra...

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Detalles Bibliográficos
Autores principales: Chu, Xujun, Wang, Mengdie, Tang, Ran, Huang, Yanan, Yu, Jiaxi, Cao, Yunfeng, Zheng, Yilei, Xie, Zhiying, Deng, Jianwen, Wang, Zhi, Ma, Wei, Song, Wenjing, Wu, Yuan, Lv, He, Zhang, Wei, Wang, Zhaoxia, Yuan, Yun, Liu, Yu, Meng, Lingchao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Molecular Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596982/
https://www.ncbi.nlm.nih.gov/pubmed/36311011
http://dx.doi.org/10.3389/fnmol.2022.1003303

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596982/
https://www.ncbi.nlm.nih.gov/pubmed/36311011
http://dx.doi.org/10.3389/fnmol.2022.1003303

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