Frequency of the transthyretin Val30Met mutation in the northern Swedish population
Author:
Publisher
Informa UK Limited
Subject
Internal Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/13506129.2013.860027
Reference7 articles.
1. Family Studies of the Genetic Abnormality in Transthyretin (Prealbumin) in Portuguese Patients with Familial Amyloidotic Poly neuropathy
2. Geographical distribution of TTR met30 carriers in northern Sweden: discrepancy between carrier frequency and prevalence rate.
3. A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers
4. Genetic epidemiology of familial amyloidotic polyneuropathy (FAP)-type I in Póvoa do Varzim and Vila do Conde (north of Portugal)
5. Heterogeneity of penetrance in familial amyloid polyneuropathy, ATTR Val30Met, in the Swedish population
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3. Disease risk estimates in V30M variant transthyretin amyloidosis (A-ATTRv) from Mallorca;Orphanet Journal of Rare Diseases;2023-08-31
4. Enlarged cross-sectional area in peripheral nerves in Swedish patients with hereditary V30M transthyretin amyloidosis;Annals of Medicine;2023-08-24
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