Whole‐exome sequencing analyses in a Saudi Ischemic Stroke Cohort reveal association signals, and shows polygenic risk scores are related to Modified Rankin Scale Risk

Ischemic stroke represents a significant societal burden across the globe. Rare high penetrant monogenic variants and less pathogenic common single nucleotide polymorphisms (SNPs) have been described as being associated with risk of diseases. Genetic studies in Saudi Arabian patients offer a greater...

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Detalles Bibliográficos
Autores principales: Alkhamis, Fahad A., Alabdali, Majed M., Alsulaiman, Abdulla A., Alamri, Abdullah S., Alali, Rudaynah, Akhtar, Mohammed S., Alsalman, Sadiq A., Cyrus, Cyril, Albakr, Aishah I., Alduhalan, Anas S., Gandla, Divya, Al-Romaih, Khaldoun, Abouelhoda, Mohamed, Loza, Bao-Li, Keating, Brendan, Al-Ali, Amein K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10042957/
https://www.ncbi.nlm.nih.gov/pubmed/36973604
http://dx.doi.org/10.1007/s10142-023-01039-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10042957/
https://www.ncbi.nlm.nih.gov/pubmed/36973604
http://dx.doi.org/10.1007/s10142-023-01039-7

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