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

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

Research output: Contribution to journalArticle

237 Scopus citations
Original languageAmerican English
Pages (from-to)410-414
Number of pages5
JournalNature Genetics
DOIs
StatePublished - 1 Jan 2002
Externally publishedYes

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    Hoffmann, K., Dreger, C. K., Olins, A. L., Olins, D. E., Shultz, L. D., Lucke, B., Karl, H., Kaps, R., Müller, D., Vayá, A., Aznar, J., Ware, R. E., Sotelo Cruz, N., Lindner, T. H., Herrmann, H., Reis, A., & Sperling, K. (2002). Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly). Nature Genetics, 410-414. https://doi.org/10.1038/ng925