Exome sequencing reveals genetic heterogeneity and clinically actionable findings in children with cerebral palsy-Reference-Cited by-同舟云学术

Exome sequencing reveals genetic heterogeneity and clinically actionable findings in children with cerebral palsy

Published:2024-05 Issue:5 Volume:30 Page:1395-1405
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Wang Yangong,Xu Yiran,Zhou Chongchen,Cheng Ye^ORCID,Qiao Niu,Shang Qing,Xia Lei,Song Juan,Gao Chao,Qiao Yimeng,Zhang Xiaoli,Li Ming,Ma Caiyun,Fan Yangyi,Peng Xirui,Wu Silin^ORCID,Lv Nan,Li Bingbing,Sun Yanyan,Zhang Bohao,Li Tongchuan,Li Hongwei,Zhang Jin,Su Yu,Li Qiaoli,Yuan Junying,Liu Lei,Moreno-De-Luca Andres^ORCID,MacLennan Alastair H.,Gecz Jozef^ORCID,Zhu Dengna,Wang Xiaoyang,Zhu Changlian^ORCID,Xing Qinghe^ORCID

Publisher

Springer Science and Business Media LLC

Link

https://www.nature.com/articles/s41591-024-02912-z.pdf

Reference72 articles.

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2. Lee, R. W. et al. A diagnostic approach for cerebral palsy in the genomic era. Neuromolecular Med. 16, 821–844 (2014).

3. Beysen, D. et al. Genetic testing contributes to diagnosis in cerebral palsy: Aicardi-Goutieres syndrome as an example. Front Neurol. 12, 617813 (2021).

4. Chang, M. J., Ma, H. I. & Lu, T. H. Estimating the prevalence of cerebral palsy in Taiwan: a comparison of different case definitions. Res. Dev. Disabil. 36C, 207–212 (2015).

5. MacLennan, A. H., Thompson, S. C. & Gecz, J. Cerebral palsy: causes, pathways, and the role of genetic variants. Am. J. Obstet. Gynecol. 213, 779–788 (2015).

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