Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report

Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report

Abstract 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 protei...

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Bibliographic Details
Main Authors: Alice Poisson, Nicolas Chatron, Audrey Labalme, Pierre Fourneret, Dorothée Ville, Marie Laure Mathieu, Damien Sanlaville, Caroline Demily, Gaëtan Lesca
Format: Article
Language:English
Published: BMC 2020-01-01
Series:BMC Medical Genetics
Subjects:
Schizophrenia
Childhood onset schizophrenia
CHD2
Genetic counselling
Chromatin
Chromodomain helicase DNA-binding
Online Access:https://doi.org/10.1186/s12881-019-0946-0

Internet

https://doi.org/10.1186/s12881-019-0946-0

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