A carregar...
A critical role for the chromatin remodeller CHD7 in anterior mesoderm during cardiovascular development
CHARGE syndrome is caused by spontaneous loss-of-function mutations to the ATP-dependant chromatin remodeller chromodomain-helicase-DNA-binding protein 7 (CHD7). It is characterised by a distinct pattern of congenital anomalies, including cardiovascular malformations. Disruption to the neural crest...
Na minha lista:
| Publicado no: | Dev Biol |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2015
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4534312/ https://ncbi.nlm.nih.gov/pubmed/26102480 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ydbio.2015.06.017 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|