Expanding the Phenotypic and Functional Evidence for KCNK3 as a Neurodevelopmental Disorder Gene: A New Chinese Case and Drosophila Validation.
- DOI
- 10.1111/cge.70216
- Published
- 2026 Oct
- Container
- Clinical genetics
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1111/cge.70216,
title = {Expanding the Phenotypic and Functional Evidence for KCNK3 as a Neurodevelopmental Disorder Gene: A New Chinese Case and Drosophila Validation.},
author = {Sun Y and Wang L and Zhang L and Gu C and Zhai C and Wang H and Chen J and Liu X and Ma X and Zhang S and Li D and Shu J and Cai C},
year = {2026},
journal = {Clinical genetics},
doi = {10.1111/cge.70216},
url = {https://doi.org/10.1111/cge.70216}
}RIS
TY - JOUR TI - Expanding the Phenotypic and Functional Evidence for KCNK3 as a Neurodevelopmental Disorder Gene: A New Chinese Case and Drosophila Validation. AU - Sun Y AU - Wang L AU - Zhang L AU - Gu C AU - Zhai C AU - Wang H AU - Chen J AU - Liu X AU - Ma X AU - Zhang S AU - Li D AU - Shu J AU - Cai C PY - 2026 JO - Clinical genetics DO - 10.1111/cge.70216 UR - https://doi.org/10.1111/cge.70216 ER -
APA
Y, S., L, W., L, Z., C, G., C, Z., H, W., J, C., X, L., X, M., S, Z., D, L., J, S., & C, C. (2026). Expanding the Phenotypic and Functional Evidence for KCNK3 as a Neurodevelopmental Disorder Gene: A New Chinese Case and Drosophila Validation.. Clinical genetics. https://doi.org/10.1111/cge.70216
Source records
- pubmed · retrieved 2026-09-26T18:12:47.266Z
- europe-pmc · retrieved 2026-09-26T18:12:47.278Z