Novel Homozygous Nonsense Mutation in the P5 ' N-1 Coding Gene as an Alternative Cause for Hereditary Anemia with Basophilic Stippling

AuthID
 P-00W-V51
10
Author(s)
Kirschner, M
·
Heinen, IR
·
Koschmieder, S
·
Bento, C
·
Eggermann, T
·
Kurth, I
·
Jost, E
·
Brummendorf, TH
·
Fuchs, R
Tipo de Documento
Article
Year published
2022
Publicado
in CLINICAL CASE REPORTS, ISSN: 2050-0904
Volume: 10, Número: 3
Indexing
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Publication Identifiers
Pubmed: 35280089
Wos: WOS:000818987200058
Source Identifiers
ISSN: 2050-0904
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