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
Publicado en:Kidney Int Rep
Main Authors: 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: Artigo
Idioma:Inglês
Publicado: Elsevier 2016
Assuntos:
Translational Research
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5678610/
https://ncbi.nlm.nih.gov/pubmed/29142973
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ekir.2016.11.005
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