Genes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression

Intellectual disability (ID), autism, and epilepsy share frequent yet variable comorbidities with one another. In order to better understand potential genetic divergence underlying this variable risk, we studied genes responsible for monogenic IDs, grouped according to their autism and epilepsy como...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: Manuel Casanova, Julia L. Sharp, Hrishikesh Chakraborty, Nahid Sultana Sumi, Manuel F. Casanova
Natura: Artigo
Lingua:inglese
Pubblicazione: 2016
Accesso online:https://doi.org/10.1186/s13229-016-0082-z
https://molecularautism.biomedcentral.com/track/pdf/10.1186/s13229-016-0082-z
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne!!