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Autism‐linked CHD gene expression patterns during development predict multi‐organ disease phenotypes
Recent large‐scale exome sequencing studies have identified mutations in several members of the CHD (Chromodomain Helicase DNA‐binding protein) gene family in neurodevelopmental disorders. Mutations in the CHD2 gene have been linked to developmental delay, intellectual disability, autism and seizure...
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| Publicado no: | J Anat |
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| Principais autores: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6231164/ https://ncbi.nlm.nih.gov/pubmed/30277262 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/joa.12889 |
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