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pro vyhledávání: '"Raimann, Bernadette"'
Autor:
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
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 2234, p 2234 (2020)
Journal of Clinical Medicine
Volume 9
Issue 7
Journal of Clinical Medicine
Volume 9
Issue 7
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::bdc0af00a29c504468d126b98e9edc03
https://www.mdpi.com/2077-0383/9/7/2234
https://www.mdpi.com/2077-0383/9/7/2234
