Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger–Huët anomaly)
Year: 2002
Type: article
Study design: Observational Study
Source: Nature Genetics
DOI: 10.1038/ng925
Institutions: Max Delbrück Center, Humboldt-Universität zu Berlin, Charité – Universitätsmedizin Berlin, German Cancer Research Center, Bowdoin College, Foundation for Blood Research, Jackson Laboratory, German Red Cross, Klinikum Chemnitz, Hospital Universitari i Politècnic La Fe, Duke Medical Center, Universitätsklinikum Würzburg, Friedrich-Alexander-Universität Erlangen-Nürnberg
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2148302734
