sábado, 23 de noviembre de 2019

Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders | Genome Medicine | Full Text

Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders | Genome Medicine | Full Text

Novel method for epilepsy phenotypes

Fereydoun Hormozdiari and colleagues present MAGI-S, a method to differentiate epilepsy phenotypes from other neurodevelopmental disorders. 

No hay comentarios:

Publicar un comentario