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The First Argentinian Family with Familial Amyloidosis of the Finnish Type
Familial amyloidosis of the Finnish type or Meretoja syndrome is a rare autosomic dominant inherited systemic condition. It was first described by Meretoja in Finland in 1969. It is a disease produced by a single mutation in the gene coding for gelsolin, which generates an abnormal protein that cumu...
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| 發表在: | Case Rep Ophthalmol |
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| Main Authors: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
S. Karger AG
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5597921/ https://ncbi.nlm.nih.gov/pubmed/28924445 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000479729 |
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