The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development

BACKGROUND: Heterozygous mutations in the chromatin remodeling gene CHD7 cause CHARGE syndrome, a developmental disorder with variable craniofacial dysmorphisms and respiratory difficulties. The molecular etiologies of these malformations are not well understood. Homozygous Chd7 null mice die by E11...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Sperry, Ethan D., Hurd, Elizabeth A., Durham, Mark A., Reamer, Elyse N., Stein, Adam B., Martin, Donna M.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2014
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4160830/
https://ncbi.nlm.nih.gov/pubmed/24975120
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvdy.24156
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