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Clinical Presentation, Diagnosis and Treatment of TTR Amyloidosis
Systemic amyloidosis can be hereditary or acquired with autosomal dominant mutations in the transthyretin gene (TTR) being the most common cause of hereditary amyloidosis. ATTRm amyloidosis is a multi-system disorder with cardiovascular, peripheral and autonomic nerve involvement that can be difficu...
Uloženo v:
| Vydáno v: | J Neuromuscul Dis |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
IOS Press
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6598024/ https://ncbi.nlm.nih.gov/pubmed/30829617 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JND-180371 |
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