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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Dades bibliogràfiques
Publicat a:Kidney Int Rep
Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: Elsevier 2016
Matèries:
Translational Research
Accés en línia: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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