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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Pubblicato in:BMC Med Genet
Autori principali: Poisson, Alice, Chatron, Nicolas, Labalme, Audrey, Fourneret, Pierre, Ville, Dorothée, Mathieu, Marie Laure, Sanlaville, Damien, Demily, Caroline, Lesca, Gaëtan
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2020
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Case Report
Accesso online: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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