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Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report
BACKGROUND: The role of deleterious copy number variations in schizophrenia is well established while data regarding pathogenic variations remain scarce. We report for the first time a case of schizophrenia in a child with a pathogenic mutation of the chromodomain helicase DNA binding protein 2 (CHD...
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| Publicado no: | BMC Med Genet |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6950831/ https://ncbi.nlm.nih.gov/pubmed/31914951 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-019-0946-0 |
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