Carregant...
Enrichment of mutations in chromatin regulators in people with Rett Syndrome lacking mutations in MECP2
PURPOSE: Rett Syndrome (RTT) is a neurodevelopmental disorder caused primarily by de novo mutations (DNMs) in MECP2 and sometimes in CDKL5 and FOXG1. However, some RTT cases lack mutations in these genes. METHODS: Twenty-two RTT cases without apparent MECP2, CDKL5, and FOXG1 mutations were subjected...
Guardat en:
| Publicat a: | Genet Med |
|---|---|
| Autors principals: | , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2016
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5107176/ https://ncbi.nlm.nih.gov/pubmed/27171548 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2016.42 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|