Asperger syndrome and early-onset schizophrenia associated with a novel MECP2 deleterious missense variant

Methyl-CpG-binding protein 2 (MECP2) deleterious variants, which are responsible for Rett syndrome in girls, are involved in a wide spectrum of developmental disabilities in males. A neuropsychiatric phenotype without intellectual disability is uncommon in patients with MECP2 deleterious variants. W...

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Veröffentlicht in:	Psychiatric genetics 2017-06, Vol.27 (3), p.105-109
Hauptverfasser:	Curie, Aurore, Lesca, Gaëtan, Bussy, Gérald, Manificat, Sabine, Arnaud, Valérie, Gonzalez, Sibylle, Revol, Olivier, Calender, Alain, Gérard, Daniel, des Portes, Vincent
Format:	Artikel
Sprache:	eng
Schlagworte:	Asperger Syndrome - genetics Asperger Syndrome - metabolism Autistic Disorder - genetics Child Genetic Predisposition to Disease - genetics Humans Intellectual Disability - genetics Male Methyl-CpG-Binding Protein 2 - genetics Methyl-CpG-Binding Protein 2 - metabolism Mutation Mutation, Missense - genetics Schizophrenia - genetics Schizophrenia, Childhood - genetics
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