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Cardiac involvement and clinical follow up of patients with hereditary transthyretin related amyloidosis associated with Glu89Gln mutation

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Bibliografske podrobnosti
izdano v:Orphanet J Rare Dis
Main Authors: Gospodinova, Mariana, Sarafov, Stayko, Guergueltcheva, Velina, Kirov, Andrey, Chamova, Teodora, Todorova, Albena, Tournev, Ivailo, Denchev, Stefan
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2015
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4642093/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-10-S1-P54
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