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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Detalhes bibliográficos
Publicado no: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 em: Elsevier 2016
Assuntos:
Translational Research
Acesso em linha: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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