A homozygous lamin B receptor variant resulting in Pelger–Huët anomaly without skeletal dysplasia

Katrin Hoffmann, Amparo Vayá, José M. Ricart Vayá, Oliver Küchler, Axel Schmidt, Nicolai von Kügelgen, Björn Fischer-Zirnsak, Karl Sperling

Open source

DOI: 10.1080/19491034.2026.2720062
Published: 2026-08-20
Container: Nucleus
Publisher: Informa UK Limited
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1080/19491034.2026.2720062,
  title = {A homozygous lamin B receptor variant resulting in Pelger–Huët anomaly without skeletal dysplasia},
  author = {Katrin Hoffmann and Amparo Vayá and José M. Ricart Vayá and Oliver Küchler and Axel Schmidt and Nicolai von Kügelgen and Björn Fischer-Zirnsak and Karl Sperling},
  year = {2026},
  journal = {Nucleus},
  doi = {10.1080/19491034.2026.2720062},
  url = {https://doi.org/10.1080/19491034.2026.2720062}
}

RIS

TY  - JOUR
TI  - A homozygous lamin B receptor variant resulting in Pelger–Huët anomaly without skeletal dysplasia
AU  - Katrin Hoffmann
AU  - Amparo Vayá
AU  - José M. Ricart Vayá
AU  - Oliver Küchler
AU  - Axel Schmidt
AU  - Nicolai von Kügelgen
AU  - Björn Fischer-Zirnsak
AU  - Karl Sperling
PY  - 2026
JO  - Nucleus
DO  - 10.1080/19491034.2026.2720062
UR  - https://doi.org/10.1080/19491034.2026.2720062
ER  -

APA

Hoffmann, K., Vayá, A., Vayá, J. M. R., Küchler, O., Schmidt, A., Kügelgen, N. V., Fischer-Zirnsak, B., & Sperling, K. (2026). A homozygous lamin B receptor variant resulting in Pelger–Huët anomaly without skeletal dysplasia. Nucleus. https://doi.org/10.1080/19491034.2026.2720062

Source records

crossref · retrieved 2026-09-26T23:02:37.918Z