Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia.

Chaumette, Boris; Ferrafiat, Vladimir; Ambalavanan, Amirthagowri; Goldenberg, Alice; Dionne-Laporte, Alexandre; Spiegelman, Dan; Dion, Patrick A; Gerardin, Priscille; Laurent, Claudine; Cohen, David; Rapoport, Judith; Rouleau, Guy A

Chaumette, Boris; Ferrafiat, Vladimir; Ambalavanan, Amirthagowri; Goldenberg, Alice; Dionne-Laporte, Alexandre; Spiegelman, Dan; Dion, Patrick A; Gerardin, Priscille; Laurent, Claudine; Cohen, David; Rapoport, Judith; Rouleau, Guy A.

Afiliação

Chaumette B; Montreal Neurological Institute and Hospital, Department of Neurology and Neurosurgery, McGill University, Montreal, QC, Canada.
Ferrafiat V; Department of Child and Adolescent Psychiatry, CHU Rouen, Rouen, France.
Ambalavanan A; Centre Référent Maladies Rares à Expression Psychiatrique, CHU Rouen, Rouen, France.
Goldenberg A; Department of Child and Adolescent Psychiatry, Arthur Rimbaud, CH Sotteville les Rouen, Rouen, France.
Dionne-Laporte A; Department of Human Genetics, McGill University, Montreal, QC, Canada.
Spiegelman D; Centre Référent Maladies Rares à Expression Psychiatrique, CHU Rouen, Rouen, France.
Dion PA; Service de génétique, CHU de Rouen, Centre Normand de Génomique Médicale et Médecine Personnalisée, Rouen, France.
Gerardin P; Montreal Neurological Institute and Hospital, Department of Neurology and Neurosurgery, McGill University, Montreal, QC, Canada.
Laurent C; Montreal Neurological Institute and Hospital, Department of Neurology and Neurosurgery, McGill University, Montreal, QC, Canada.
Cohen D; Montreal Neurological Institute and Hospital, Department of Neurology and Neurosurgery, McGill University, Montreal, QC, Canada.
Rapoport J; Department of Child and Adolescent Psychiatry, CHU Rouen, Rouen, France.
Rouleau GA; Centre Référent Maladies Rares à Expression Psychiatrique, CHU Rouen, Rouen, France.

Mol Psychiatry ; 25(4): 821-830, 2020 04.

Article em En | MEDLINE | ID: mdl-29895895

Assuntos

Proteínas de Membrana/genética; Fosfoproteínas/genética; Esquizofrenia Infantil/genética; ATPase Trocadora de Sódio-Potássio/genética; Pré-Escolar; Feminino; Humanos; Lactente; Masculino; Proteínas de Membrana/metabolismo; Mutação/genética; Mutação de Sentido Incorreto/genética; Fosfoproteínas/metabolismo; Esquizofrenia Infantil/fisiopatologia; ATPase Trocadora de Sódio-Potássio/metabolismo

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fosfoproteínas / Esquizofrenia Infantil / ATPase Trocadora de Sódio-Potássio / Proteínas de Membrana Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google