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TY  - JOUR
AU  - Kirschner, Martin
AU  - Heinen, Inga Rebecca
AU  - Koschmieder, Steffen
AU  - Manco, Licinio
AU  - Bento, Celeste
AU  - Eggermann, Thomas
AU  - Kurth, Ingo
AU  - Jost, Edgar
AU  - Brümmendorf, Tim Henrik
AU  - Fuchs, Roland
TI  - Novel homozygous nonsense mutation in the P5′N-1 coding gene as an alternative cause for hereditary anemia with basophilic stippling
JO  - Clinical Case Reports
VL  - 10
IS  - 3
SN  - 2050-0904
CY  - Chichester
PB  - Wiley
M1  - RWTH-CONV-249536
SP  - e05501
PY  - 2022
LB  - PUB:(DE-HGF)16
UR  - <Go to ISI:>//WOS:000818987200058
C6  - pmid:35280089
DO  - DOI:10.1002/ccr3.5501
UR  - https://publications.rwth-aachen.de/record/856502
ER  -