A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome.
- DOI
- 10.1002/ccr3.72218
- Published
- 2026 Mar
- Container
- Clinical case reports
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1002/ccr3.72218,
title = {A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome.},
author = {Arefzadeh M and Rabbani B and Abdolahpour S and Emami F and Abbasi F and Masoumi T and Mirab Samiee S and Rabbani A and Mahdieh N},
year = {2026},
journal = {Clinical case reports},
doi = {10.1002/ccr3.72218},
url = {https://doi.org/10.1002/ccr3.72218}
}RIS
TY - JOUR TI - A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome. AU - Arefzadeh M AU - Rabbani B AU - Abdolahpour S AU - Emami F AU - Abbasi F AU - Masoumi T AU - Mirab Samiee S AU - Rabbani A AU - Mahdieh N PY - 2026 JO - Clinical case reports DO - 10.1002/ccr3.72218 UR - https://doi.org/10.1002/ccr3.72218 ER -
APA
M, A., B, R., S, A., F, E., F, A., T, M., S, M. S., A, R., & N, M. (2026). A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome.. Clinical case reports. https://doi.org/10.1002/ccr3.72218
Source records
- pubmed · retrieved 2026-09-25T00:30:43.320Z