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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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Detalhes bibliográficos
Publicado no:J Anat
Principais autores: Kasah, Sahrunizam, Oddy, Christopher, Basson, M. Albert
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2018
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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