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.

Dades bibliogràfiques
Autors principals: Saja, K, Bignell, P, Robson, K, Provan, D
Format: Journal article
Idioma:English
Publicat: 2010