Precise Therapeutic Targeting of Distinct NRXN1(+/−) Mutations

As genetic studies continue to identify risk loci that are significantly associated with risk for neuropsychiatric disease, a critical unanswered question is the extent to which diverse mutations --sometimes impacting the same gene-- will require common or individually tailored therapeutic strategie...

Descripción completa

Detalles Bibliográficos
Autores principales: Fernando, Michael B., Fan, Yu, Zhang, Yanchun, Kammourh, Sarah, Murphy, Aleta N., Ghorbani, Sadaf, Onatzevitch, Ryan, Pero, Adriana, Padilla, Christopher, Cao, Lei, Williams, Sarah, Fang, Gang, Slesinger, Paul A., Brennand, Kristen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634884/
https://www.ncbi.nlm.nih.gov/pubmed/37961635
http://dx.doi.org/10.1101/2023.10.28.564543

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634884/
https://www.ncbi.nlm.nih.gov/pubmed/37961635
http://dx.doi.org/10.1101/2023.10.28.564543

Ejemplares similares