Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Tale N. Wien"'
Autor:
Dorota Rowczenio, Maria Stensland, Gustavo A. de Souza, Erik H. Strøm, Janet A. Gilbertson, Graham Taylor, Nigel Rendell, Shane Minogue, Yvonne A. Efebera, Helen J. Lachmann, Ashutosh D. Wechalekar, Philip N. Hawkins, Ketil R. Heimdal, Kristian Selvig, Inger K. Lægreid, Nathalie Demoulin, Selda Aydin, Julian D. Gillmore, Tale N. Wien
Publikováno v:
Kidney International Reports, Vol 2, Iss 3, Pp 461-469 (2017)
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 kid
Externí odkaz:
https://doaj.org/article/eafc8316f25e41acb96af87f66ab9d68
