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.

Detalhes bibliográficos
Principais autores:	Saja, K, Bignell, P, Robson, K, Provan, D
Formato:	Journal article
Idioma:	English
Publicado em:	2010

A novel missense mutation c.470 A&gt;C (p.D157A) in the SLC40A1 gene as a cause of ferroportin disease in a family with hyperferritinaemia.