Novel homozygous nonsense mutation in the P5′N‐1 coding gene as an alternative cause for hereditary anemia with basophilic stippling. - Kirschner, Martin; Heinen, Inga Rebecca; Koschmieder, Steffen; Manco, Licinio; Bento, Celeste; Eggermann, Thomas; Kurth, Ingo; Jost, Edgar; Brümmendorf, Tim H.; Fuchs, Roland (Clinical Case Reports, 2022)