Lack of association of TP73 rare variants with amyotrophic lateral sclerosis in a Chinese cohort

BACKGROUND: Recently, several rare variants of TP73 were identified as potential disease cause for amyotrophic lateral sclerosis (ALS) in the European population. However, further replication was still necessary, especially in cohorts with different ethnic backgrounds. METHODS: To explore the geneti...

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Detalles Bibliográficos
Autores principales: Li, Chunyu, Hou, Yanbing, Wei, Qianqian, Lin, Junyu, Jiang, Qirui, Yang, Tianmi, Xiao, Yi, Huang, Jingxuan, Cheng, Yangfan, Ou, Ruwei, Liu, Kuncheng, Chen, Xueping, Song, Wei, Zhao, Bi, Wu, Ying, Cao, Bei, Chen, Yongping, Shang, Huifang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Correspondence
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710084/
https://www.ncbi.nlm.nih.gov/pubmed/36451215
http://dx.doi.org/10.1186/s40246-022-00437-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9710084/
https://www.ncbi.nlm.nih.gov/pubmed/36451215
http://dx.doi.org/10.1186/s40246-022-00437-5

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