Hereditary Transthyretin Amyloidosis in Eight Chinese Families

BACKGROUND: Mutations of transthyretin (TTR) cause the most common type of autosomal-dominant hereditary systemic amyloidosis, which occurs worldwide. To date, more and more mutations in the TTR gene have been reported. Some variations in the clinical presentation are often observed in patients with...

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Detalles Bibliográficos
Autores principales: Meng, Ling-Chao, Lyu, He, Zhang, Wei, Liu, Jing, Wang, Zhao-Xia, Yuan, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756886/
https://www.ncbi.nlm.nih.gov/pubmed/26521788
http://dx.doi.org/10.4103/0366-6999.168048

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756886/
https://www.ncbi.nlm.nih.gov/pubmed/26521788
http://dx.doi.org/10.4103/0366-6999.168048

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