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Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger–Huët anomaly)

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Year: 2002
Type: article
Study design: Observational Study
Source: Nature Genetics
DOI: 10.1038/ng925
Authors: Katrin Hoffmann, Christine K. Dreger, Ada L. Olins, Donald E. Olins, Leonard D. Shultz, Barbara Lucke, Hartmut Karl, Reinhard Kaps, Dietmar Müller, Amparo Vayá, Justo Aznar, Russell E. Ware, Norberto Sotelo Cruz, Tom H. Lindner, Harald Herrmann, André Reis, Karl Sperling
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

Topic: Nuclear Structure and Function
Subfield: Molecular Biology
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W2148302734
FWCI: 5.966
Cites: 25
Cited by: 345
Related to: 10
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