The recurrent WASF1 nonsense variant identified in two unaffected Chinese families with neurodevelopmental disorder: case report and review of the literatures
- DOI
- 10.1186/s12920-023-01630-8
- Published
- 2023-08-28
- Container
- BMC Medical Genomics
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1186/s12920-023-01630-8,
title = {The recurrent WASF1 nonsense variant identified in two unaffected Chinese families with neurodevelopmental disorder: case report and review of the literatures},
author = {Xiang Tang and Guoqing Liu and Li Lin and Nong Xiao and Yuxia Chen},
year = {2023},
journal = {BMC Medical Genomics},
doi = {10.1186/s12920-023-01630-8},
url = {https://doi.org/10.1186/s12920-023-01630-8}
}RIS
TY - JOUR TI - The recurrent WASF1 nonsense variant identified in two unaffected Chinese families with neurodevelopmental disorder: case report and review of the literatures AU - Xiang Tang AU - Guoqing Liu AU - Li Lin AU - Nong Xiao AU - Yuxia Chen PY - 2023 JO - BMC Medical Genomics DO - 10.1186/s12920-023-01630-8 UR - https://doi.org/10.1186/s12920-023-01630-8 ER -
APA
Tang, X., Liu, G., Lin, L., Xiao, N., & Chen, Y. (2023). The recurrent WASF1 nonsense variant identified in two unaffected Chinese families with neurodevelopmental disorder: case report and review of the literatures. BMC Medical Genomics. https://doi.org/10.1186/s12920-023-01630-8
Source records
- crossref · retrieved 2026-11-05T04:58:11.518Z