Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3)
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M. Cazzola | M. Ferrari | R. Paroni | L. Cremonesi | P. Arosio | M. Papaioannou | S. Levi | N. Soriani | J. Christakis | A. Charalambidou | K. Romtsou | A. Kioumi