Deciphering TCOF1 mutations in Chinese Treacher Collins syndrome patients: insights into pathogenesis and transcriptional disruption.
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| Title: | Deciphering TCOF1 mutations in Chinese Treacher Collins syndrome patients: insights into pathogenesis and transcriptional disruption. |
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| Authors: | Jiang, Zhuoyuan1 (AUTHOR), Mao, Ke1 (AUTHOR), Wang, Bingqing2 (AUTHOR), Zhu, Hao1 (AUTHOR), Liu, Jiqiang1 (AUTHOR), Lang, Ruirui1 (AUTHOR), Xiao, Baichuan1 (AUTHOR), Shan, Hailin1 (AUTHOR), Chen, Qi2 (AUTHOR), Li, Ying3 (AUTHOR), Zhao, Shouqin3 (AUTHOR), Zhang, Qingguo2 (AUTHOR), Liu, Huisheng4,5 (AUTHOR) liu_huisheng@grmh-gdl.cn, Zhang, Yong-Biao1,6 (AUTHOR) zhangyongbiao@buaa.edu.cn |
| Source: | Orphanet Journal of Rare Diseases. 2/7/2025, Vol. 20 Issue 1, p1-12. 12p. |
| Database: | Academic Search Ultimate |
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