Management of asymptomatic gene carriers of transthyretin familial amyloid polyneuropathy

Transthyretin familial amyloid polyneuropathy (TTR‐FAP) is a rare, severe, and irreversible, adult‐onset, hereditary disorder caused by autosomal‐dominant mutations in the TTR gene that increase the intrinsic propensity of transthyretin protein to misfold and deposit systemically as insoluble amyloi...

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Detalles Bibliográficos
Autores principales: Schmidt, Hartmut H.‐J., Barroso, Fabio, González‐Duarte, Alejandra, Conceição, Isabel, Obici, Laura, Keohane, Denis, Amass, Leslie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Invited Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113802/
https://www.ncbi.nlm.nih.gov/pubmed/27273296
http://dx.doi.org/10.1002/mus.25210

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113802/
https://www.ncbi.nlm.nih.gov/pubmed/27273296
http://dx.doi.org/10.1002/mus.25210

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