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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Detalles Bibliográficos
Autores principales: Lucero Saá, Francisco, Cremona, Federico Andrés, Mínguez, Natalia Ximena, Igarzabal, María Laura, Chiaradía, Pablo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597921/
https://www.ncbi.nlm.nih.gov/pubmed/28924445
http://dx.doi.org/10.1159/000479729

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597921/
https://www.ncbi.nlm.nih.gov/pubmed/28924445
http://dx.doi.org/10.1159/000479729

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