Autosomal dominant gain-of-function mutations in LCP1 cause a syndromic neutropenia and immunodeficiency.
- DOI
- 10.1016/j.gendis.2026.102232
- Published
- 2027 Jan
- Container
- Genes & diseases
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1016/j.gendis.2026.102232,
title = {Autosomal dominant gain-of-function mutations in LCP1 cause a syndromic neutropenia and immunodeficiency.},
author = {Yu L and Zhou B and Liu W and Li W and Wei Q and Zhang Y and Li C and Li W and Li Y and Li G and Sun G and Gan R and Chen R and Zhang W and Zeng A and Zhao R and He W and Jia Y and Zhou L and Zhang Z and Tang X and Qiu X and Zhou Q and Song W and Zhao X and An Y},
year = {2027},
journal = {Genes \& diseases},
doi = {10.1016/j.gendis.2026.102232},
url = {https://doi.org/10.1016/j.gendis.2026.102232}
}RIS
TY - JOUR TI - Autosomal dominant gain-of-function mutations in LCP1 cause a syndromic neutropenia and immunodeficiency. AU - Yu L AU - Zhou B AU - Liu W AU - Li W AU - Wei Q AU - Zhang Y AU - Li C AU - Li W AU - Li Y AU - Li G AU - Sun G AU - Gan R AU - Chen R AU - Zhang W AU - Zeng A AU - Zhao R AU - He W AU - Jia Y AU - Zhou L AU - Zhang Z AU - Tang X AU - Qiu X AU - Zhou Q AU - Song W AU - Zhao X AU - An Y PY - 2027 JO - Genes & diseases DO - 10.1016/j.gendis.2026.102232 UR - https://doi.org/10.1016/j.gendis.2026.102232 ER -
APA
L, Y., B, Z., W, L., W, L., Q, W., Y, Z., C, L., W, L., Y, L., G, L., G, S., R, G., R, C., W, Z., A, Z., R, Z., W, H., Y, J., L, Z., Z, Z., X, T., X, Q., Q, Z., W, S., X, Z., & Y, A. (2027). Autosomal dominant gain-of-function mutations in LCP1 cause a syndromic neutropenia and immunodeficiency.. Genes & diseases. https://doi.org/10.1016/j.gendis.2026.102232
Source records
- pubmed · retrieved 2026-09-26T20:50:33.761Z