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Article

Early-onset haemochromatosis caused by a novel combination of TFR2 mutations(p.R396X/c.1538-2 A>G) in a woman of Italian descent.

Haematologica - 1 May 2008

Gérolami V, Le Gac G, Mercier L, Nezri M, Bergé-Lefranc J-L, Férec C

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Identifiers

PMID: 18450729
DOI: 10.3324/haematol.12884

Genes

TFR2

Variants

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