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Cardiac involvement and clinical follow up of patients with hereditary transthyretin related amyloidosis associated with Glu89Gln mutation
Shranjeno v:
| izdano v: | Orphanet J Rare Dis |
|---|---|
| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2015
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| 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 |
| Oznake: |
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