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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Clin Med
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: MDPI 2020
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7408866/
https://ncbi.nlm.nih.gov/pubmed/32674397
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm9072234
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