Genetic variation within the pri-let-7f-2 in the X chromosome predicting stroke risk in a Chinese Han population from Liaoning, China: From a case-control study to a new predictive nomogram

BACKGROUND AND OBJECTIVES: Stroke is the most common cause of disability and the second cause of death worldwide. Therefore, there is a need to identify patients at risk of developing stroke. This case-control study aimed to create and verify a gender-specific genetic signature-based nomogram to fac...

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Detalles Bibliográficos
Autores principales: Wang, Yaxuan, Qiu, Luying, Wang, Yuye, He, Zhiyi, Lan, Xue, Cui, Lei, Wang, Yanzhe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747750/
https://www.ncbi.nlm.nih.gov/pubmed/36530894
http://dx.doi.org/10.3389/fmed.2022.936249

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747750/
https://www.ncbi.nlm.nih.gov/pubmed/36530894
http://dx.doi.org/10.3389/fmed.2022.936249

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