Missense Variants Reveal Functional Insights Into the Human ARID Family of Gene Regulators

Missense variants are alterations to protein coding sequences that result in amino acid substitutions. They can be deleterious if the amino acid is required for maintaining structure or/and function, but are likely to be tolerated at other sites. Consequently, missense variation within a healthy pop...

Descripción completa

Detalles Bibliográficos
Autores principales: Deák, Gauri, Cook, Atlanta G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9077328/
https://www.ncbi.nlm.nih.gov/pubmed/35257783
http://dx.doi.org/10.1016/j.jmb.2022.167529

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9077328/
https://www.ncbi.nlm.nih.gov/pubmed/35257783
http://dx.doi.org/10.1016/j.jmb.2022.167529

Ejemplares similares