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Epistatic interactions between Chd7 and Fgf8 during cerebellar development: Implications for CHARGE syndrome
CHARGE syndrome is a rare, autosomal dominant condition caused by mutations in the CHD7 gene. Although central nervous system defects have been reported, the detailed description and analysis of these anomalies in CHARGE syndrome patients lag far behind the description of other, more easily observed...
Tallennettuna:
| Päätekijä: | |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Landes Bioscience
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4091603/ https://ncbi.nlm.nih.gov/pubmed/25054096 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/rdis.28688 |
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