Novel homozygous nonsense mutation in the P5′N-1 coding gene as an alternative cause for hereditary anemia with basophilic stippling

Kirschner, Martin; Bento, Celeste; Fuchs, Roland; Koschmieder, Steffen; Jost, Edgar; Kurth, Ingo; Heinen, Inga Rebecca; Brümmendorf, Tim Henrik; Manco, Licinio; Eggermann, Thomas

doi:10.18154/RWTH-CONV-249536

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Novel homozygous nonsense mutation in the P5′N-1 coding gene as an alternative cause for hereditary anemia with basophilic stippling - RWTH-CONV-249536

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