Hoppa till innehåll
VuFind
English
Deutsch
Español
Français
Italiano
日本語
Nederlands
Português
Português (Brasil)
中文(简体)
中文(繁體)
Türkçe
עברית
Gaeilge
Cymraeg
Ελληνικά
Català
Euskara
Русский
Čeština
Suomi
Svenska
polski
Dansk
slovenščina
اللغة العربية
বাংলা
Galego
Tiếng Việt
Hrvatski
हिंदी
Հայերէն
Українська
Sámegiella
Монгол
Språk
Alla fält
Titel
Upphovsman
Ämne
Signum
ISBN/ISSN
Tagg
Sök
Avancerad
A novel missense mutation c.47...
Hänvisa
Textmeddelande
Skicka per e-post
Skriv ut
Exportera posten
Exportera till: RefWorks
Exportera till: EndNoteWeb
Exportera till: EndNote
Permanent länk
A novel missense mutation c.470 A>C (p.D157A) in the SLC40A1 gene as a cause of ferroportin disease in a family with hyperferritinaemia.
Bibliografiska uppgifter
Huvudupphovsmän:
Saja, K
,
Bignell, P
,
Robson, K
,
Provan, D
Materialtyp:
Journal article
Språk:
English
Publicerad:
2010
Beståndsuppgifter
Beskrivning
Liknande verk
Katalogiseringsuppgifter
Liknande verk
Transmembrane protein western blotting: Impact of sample preparation on detection of SLC11A2 (DMT1) and SLC40A1 (ferroportin).
av: Yoshiaki Tsuji
Publicerad: (2020-01-01)
Phenotype of Usher syndrome type II assosiated with compound missense mutations of c.721 C>T and c.1969 C>T in MYO7A in a Chinese Usher syndrome family
av: Wei Zhai, et al.
Publicerad: (2015-08-01)
Role of liver magnetic resonance imaging in hyperferritinaemia and the diagnosis of iron overload
av: Axel Rüfer, et al.
Publicerad: (2017-11-01)
PO.2.51 Hyperferritinaemia and systemic disease : SLE or still’s disease?
av: N Bouziani, et al.
Publicerad: (2022-10-01)
Duodenal ferroportin is up-regulated in patients with chronic hepatitis C.
av: Lanqing Ma, et al.
Publicerad: (2014-01-01)