Hereditary ATTR Amyloidosis in Austria: Prevalence and Epidemiological Hot Spots

Background: Hereditary transthyretin amyloidosis (hATTR) is an autosomal dominantly inherited disorder caused by an accumulation of amyloid fibrils in tissues due to mutations in the transthyretin (TTR) gene. The prevalence of hATTR is still unclear and likely underestimated in many countries. In or...

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Detalles Bibliográficos
Autores principales: Auer-Grumbach, Michaela, Rettl, Rene, Ablasser, Klemens, Agis, Hermine, Beetz, Christian, Duca, Franz, Gattermeier, Martin, Glaser, Franz, Hacker, Markus, Kain, Renate, Kaufmann, Birgit, Kovacs, Gabor G., Lampl, Christian, Ljevakovic, Neira, Nagele, Jutta, Pölzl, Gerhard, Quasthoff, Stefan, Raimann, Bernadette, Rauschka, Helmut, Reiter, Christian, Skrahina, Volha, Schuhfried, Othmar, Sunder-Plassmann, Raute, Verheyen, Nicolas D., Wanschitz, Julia, Weber, Thomas, Windhager, Reinhard, Wurm, Raphael, Zimprich, Friedrich, Löscher, Wolfgang N., Bonderman, Diana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408866/
https://www.ncbi.nlm.nih.gov/pubmed/32674397
http://dx.doi.org/10.3390/jcm9072234

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408866/
https://www.ncbi.nlm.nih.gov/pubmed/32674397
http://dx.doi.org/10.3390/jcm9072234

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