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Ocular Involvement in Hereditary Amyloidosis
The term amyloidosis describes a group of rare diseases caused by protein conformation abnormalities resulting in extracellular deposition and accumulation of insoluble fibrillar aggregates. So far, 36 amyloid precursor proteins have been identified, and each one is responsible for a specific diseas...
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| 出版年: | Genes (Basel) |
|---|---|
| 主要な著者: | , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8304974/ https://ncbi.nlm.nih.gov/pubmed/34206500 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes12070955 |
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