Cardiac involvement and clinical follow up of patients with hereditary transthyretin related amyloidosis associated with Glu89Gln mutationReport as inadecuate




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Orphanet Journal of Rare Diseases

, 10:P54

First Online: 02 November 2015DOI: 10.1186-1750-1172-10-S1-P54

Cite this article as: Gospodinova, M., Sarafov, S., Guergueltcheva, V. et al. Orphanet J Rare Dis 2015 10Suppl 1: P54. doi:10.1186-1750-1172-10-S1-P54 Download fulltext PDF



Author: Mariana Gospodinova - Stayko Sarafov - Velina Guergueltcheva - Andrey Kirov - Teodora Chamova - Albena Todorova - Ivailo To

Source: https://link.springer.com/



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