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%0 Journal Article
%A Kirschner, Martin
%A Heinen, Inga Rebecca
%A Koschmieder, Steffen
%A Manco, Licinio
%A Bento, Celeste
%A Eggermann, Thomas
%A Kurth, Ingo
%A Jost, Edgar
%A Brümmendorf, Tim Henrik
%A Fuchs, Roland
%T Novel homozygous nonsense mutation in the P5′N-1 coding gene as an alternative cause for hereditary anemia with basophilic stippling
%J Clinical Case Reports
%V 10
%N 3
%@ 2050-0904
%C Chichester
%I Wiley
%M RWTH-CONV-249536
%P e05501
%D 2022
%F PUB:(DE-HGF)16
%9 Journal Article
%U <Go to ISI:>//WOS:000818987200058
%$ pmid:35280089
%R 10.1002/ccr3.5501
%U https://publications.rwth-aachen.de/record/856502