Carregant...
The KMT2D Kabuki syndrome histone methylase controls neural crest cell differentiation and facial morphology
Kabuki syndrome (KS) is a congenital craniofacial disorder resulting from mutations in the KMT2D histone methylase (KS1) or the UTX histone demethylase (KS2). With small cohorts of KS2 patients, it is not clear whether differences exist in clinical manifestations relative to KS1. We mutated KMT2D in...
Guardat en:
| Publicat a: | Development |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Company of Biologists Ltd
2020
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7375479/ https://ncbi.nlm.nih.gov/pubmed/32541010 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dev.187997 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|