Association of protein function-altering variants with cardiometabolic traits: the strong heart study

Clinical and biomarker phenotypic associations for carriers of protein function-altering variants may help to elucidate gene function and health effects in populations. We genotyped 1127 Strong Heart Family Study participants for protein function-altering single nucleotide variants (SNV) and indels ...

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Detalles Bibliográficos
Autores principales: Shan, Yue, Cole, Shelley A., Haack, Karin, Melton, Phillip E., Best, Lyle G., Bizon, Christopher, Kobes, Sayuko, Köroğlu, Çiğdem, Baier, Leslie J., Hanson, Robert L., Sanna, Serena, Li, Yun, Franceschini, Nora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167281/
https://www.ncbi.nlm.nih.gov/pubmed/35665752
http://dx.doi.org/10.1038/s41598-022-12866-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167281/
https://www.ncbi.nlm.nih.gov/pubmed/35665752
http://dx.doi.org/10.1038/s41598-022-12866-2

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