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Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly).
Nat Genet. 2002 Aug;31(4):410-4. doi: 10.1038/ng925. Epub 2002 Jul 15.
Nat Genet. 2002.
PMID: 12118250
Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huët anomaly.
Shultz LD, Lyons BL, Burzenski LM, Gott B, Samuels R, Schweitzer PA, Dreger C, Herrmann H, Kalscheuer V, Olins AL, Olins DE, Sperling K, Hoffmann K.
Shultz LD, et al.
Hum Mol Genet. 2003 Jan 1;12(1):61-9. doi: 10.1093/hmg/ddg003.
Hum Mol Genet. 2003.
PMID: 12490533
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Investigation of nuclear architecture with a domain-presenting expression system.
Dreger CK, König AR, Spring H, Lichter P, Herrmann H.
Dreger CK, et al.
J Struct Biol. 2002 Oct-Dec;140(1-3):100-15. doi: 10.1016/s1047-8477(02)00540-3.
J Struct Biol. 2002.
PMID: 12490158
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Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation.
Reichart B, Klafke R, Dreger C, Krüger E, Motsch I, Ewald A, Schäfer J, Reichmann H, Müller CR, Dabauvalle MC.
Reichart B, et al.
BMC Cell Biol. 2004 Mar 30;5:12. doi: 10.1186/1471-2121-5-12.
BMC Cell Biol. 2004.
PMID: 15053843
Free PMC article.
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