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

Saved in:
Bibliographic Details
Title: Novel homozygous nonsense mutation in the P5′N‐1 coding gene as an alternative cause for hereditary anemia with basophilic stippling.
Authors: Kirschner, Martin1,2 (AUTHOR) mkirschner@ukaachen.de, Heinen, Inga Rebecca1,2 (AUTHOR), Koschmieder, Steffen1,2 (AUTHOR), Manco, Licinio3 (AUTHOR), Bento, Celeste4 (AUTHOR), Eggermann, Thomas5 (AUTHOR), Kurth, Ingo5 (AUTHOR), Jost, Edgar1,2 (AUTHOR), Brümmendorf, Tim H.1,2 (AUTHOR), Fuchs, Roland1,2 (AUTHOR)
Source: Clinical Case Reports. Mar2022, Vol. 10 Issue 3, p1-6. 6p.
Database: Academic Search Ultimate
Full text is not displayed to guests.
Description
ISSN:20500904
DOI:10.1002/ccr3.5501