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.

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Hlavní autoři: Saja, K, Bignell, P, Robson, K, Provan, D
Médium: Journal article
Jazyk:English
Vydáno: 2010