Epidemiology of hereditary transthyretin amyloidosis in the northernmost region of Sweden: a retrospective cohort study
Author:
Affiliation:
1. Piteå Research Unit, Region Norrbotten, Piteå, Sweden
2. Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden
3. Wallenberg Centre for Molecular Medicine, Umeå University, Umeå, Sweden
Funder
Piteå Älvdals Hospital Foundation
the Norrbotten County Council
Publisher
Informa UK Limited
Subject
Internal Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/13506129.2022.2026323
Reference29 articles.
1. Hereditary transthyretin amyloidosis from a Scandinavian perspective
2. Heterogeneity of penetrance in familial amyloid polyneuropathy, ATTR Val30Met, in the Swedish population
3. New data on the genetic profile and penetrance of hereditary Val30Met transthyretin amyloidosis in Sweden
4. One mutation, two distinct disease variants: unravelling the impact of transthyretin amyloid fibril composition
5. Incidence of hereditary amyloidosis and autoinflammatory diseases in Sweden: endemic and imported diseases
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