Biophysical characterization and modulation of Transthyretin Ala97Ser

OBJECTIVE: Ala97Ser (A97S) is the major transthyretin (TTR) mutation in Taiwanese patients of familial amyloid polyneuropathy (FAP), characterized by a late‐onset but rapidly deteriorated neuropathy. Tafamidis can restore the stability of some mutant TTR tetramers and slow down the progression of TT...

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Detalles Bibliográficos
Autores principales: Liu, Yo‐Tsen, Yen, Yueh‐Jung, Ricardo, Frans, Chang, Yu, Wu, Pei‐Hao, Huang, Shing‐Jong, Lin, Kon‐Ping, Yu, Tsyr‐Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801203/
https://www.ncbi.nlm.nih.gov/pubmed/31502419
http://dx.doi.org/10.1002/acn3.50887

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801203/
https://www.ncbi.nlm.nih.gov/pubmed/31502419
http://dx.doi.org/10.1002/acn3.50887

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