A Novel de novo Mutation in EBF3 Associated With Hypotonia, Ataxia, and Delayed Development Syndrome in a Chinese Boy
- DOI
- 10.3389/fgene.2021.676832
- Published
- 2021-07-22
- Container
- Frontiers in Genetics
- Publisher
- Frontiers Media SA
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.3389/fgene.2021.676832,
title = {A Novel de novo Mutation in EBF3 Associated With Hypotonia, Ataxia, and Delayed Development Syndrome in a Chinese Boy},
author = {Yanru Huang and Libin Mei and Yangdan Wang and Huiming Ye and Xiaomin Ma and Jian Zhang and Meijiao Cai and Ping Li and Yunsheng Ge and Yulin Zhou},
year = {2021},
journal = {Frontiers in Genetics},
doi = {10.3389/fgene.2021.676832},
url = {https://doi.org/10.3389/fgene.2021.676832}
}RIS
TY - JOUR TI - A Novel de novo Mutation in EBF3 Associated With Hypotonia, Ataxia, and Delayed Development Syndrome in a Chinese Boy AU - Yanru Huang AU - Libin Mei AU - Yangdan Wang AU - Huiming Ye AU - Xiaomin Ma AU - Jian Zhang AU - Meijiao Cai AU - Ping Li AU - Yunsheng Ge AU - Yulin Zhou PY - 2021 JO - Frontiers in Genetics DO - 10.3389/fgene.2021.676832 UR - https://doi.org/10.3389/fgene.2021.676832 ER -
APA
Huang, Y., Mei, L., Wang, Y., Ye, H., Ma, X., Zhang, J., Cai, M., Li, P., Ge, Y., & Zhou, Y. (2021). A Novel de novo Mutation in EBF3 Associated With Hypotonia, Ataxia, and Delayed Development Syndrome in a Chinese Boy. Frontiers in Genetics. https://doi.org/10.3389/fgene.2021.676832
Source records
- crossref · retrieved 2026-11-10T10:33:49.700Z