Renal Amyloidosis Associated With 5 Novel Variants in the Fibrinogen A Alpha Chain Protein

INTRODUCTION: Fibrinogen A alpha chain amyloidosis is an autosomal dominant disease associated with mutations in the fibrinogen A alpha chain (FGA) gene, and it is the most common cause of hereditary renal amyloidosis in the UK. Patients typically present with kidney impairment and progress to end-s...

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Detalles Bibliográficos
Autores principales: Rowczenio, Dorota, Stensland, Maria, de Souza, Gustavo A., Strøm, Erik H., Gilbertson, Janet A., Taylor, Graham, Rendell, Nigel, Minogue, Shane, Efebera, Yvonne A., Lachmann, Helen J., Wechalekar, Ashutosh D., Hawkins, Philip N., Heimdal, Ketil R., Selvig, Kristian, Lægreid, Inger K., Demoulin, Nathalie, Aydin, Selda, Gillmore, Julian D., Wien, Tale N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Translational Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678610/
https://www.ncbi.nlm.nih.gov/pubmed/29142973
http://dx.doi.org/10.1016/j.ekir.2016.11.005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678610/
https://www.ncbi.nlm.nih.gov/pubmed/29142973
http://dx.doi.org/10.1016/j.ekir.2016.11.005

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