A proposed role for CDO1 in CNS development: Three children with rare missense variants and a neurological phenotype.
- DOI
- 10.1016/j.xhgg.2025.100417
- Published
- 2025 Apr 10
- Container
- HGG advances
- Publisher
- Not recorded
- Open access
- yes
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limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.1016/j.xhgg.2025.100417,
title = {A proposed role for CDO1 in CNS development: Three children with rare missense variants and a neurological phenotype.},
author = {Rowe L and Mullegama SV and Lombardo R and Barnes C and Towner S and Snyder MT and Heidlebaugh A and Riordan H and Begtrup A and Crunk A and Cui H and Dameron AE and Folk L and Guillen Sacoto MJ and Juusola J and Redlich OL and Reich A and McGivern B},
year = {2025},
journal = {HGG advances},
doi = {10.1016/j.xhgg.2025.100417},
url = {https://doi.org/10.1016/j.xhgg.2025.100417}
}RIS
TY - JOUR TI - A proposed role for CDO1 in CNS development: Three children with rare missense variants and a neurological phenotype. AU - Rowe L AU - Mullegama SV AU - Lombardo R AU - Barnes C AU - Towner S AU - Snyder MT AU - Heidlebaugh A AU - Riordan H AU - Begtrup A AU - Crunk A AU - Cui H AU - Dameron AE AU - Folk L AU - Guillen Sacoto MJ AU - Juusola J AU - Redlich OL AU - Reich A AU - McGivern B PY - 2025 JO - HGG advances DO - 10.1016/j.xhgg.2025.100417 UR - https://doi.org/10.1016/j.xhgg.2025.100417 ER -
APA
L, R., SV, M., R, L., C, B., S, T., MT, S., A, H., H, R., A, B., A, C., H, C., AE, D., L, F., MJ, G. S., J, J., OL, R., A, R., & B, M. (2025). A proposed role for CDO1 in CNS development: Three children with rare missense variants and a neurological phenotype.. HGG advances. https://doi.org/10.1016/j.xhgg.2025.100417
Source records
- pubmed · retrieved 2026-09-25T17:29:48.106Z