Epigenetic Etiology of Intellectual Disability.

Iwase, Shigeki; Bérubé, Nathalie G; Zhou, Zhaolan; Kasri, Nael Nadif; Battaglioli, Elena; Scandaglia, Marilyn; Barco, Angel

Iwase, Shigeki; Bérubé, Nathalie G; Zhou, Zhaolan; Kasri, Nael Nadif; Battaglioli, Elena; Scandaglia, Marilyn; Barco, Angel.

Afiliação

Iwase S; University of Michigan Medical School, Medical Science II, Ann Arbor, Michigan 48109-5618.
Bérubé NG; Western University and Children's Health Research Institute, Victoria Research Laboratories, London, Ontario N6C 2V5, Canada.
Zhou Z; Department of Genetics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania 19104-6145.
Kasri NN; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, 6500 HB, Nijmegen, The Netherlands.
Battaglioli E; University of Milan, Department Medical Biotechnology and Translational Medicine, 20090 Segrate (MI), Italy, and.
Scandaglia M; Instituto de Neurociencias, Molecular Neurobiology Unit, s/n 03550, San Juan de Alicante, Alicante, Spain.
Barco A; Instituto de Neurociencias, Molecular Neurobiology Unit, s/n 03550, San Juan de Alicante, Alicante, Spain abarco@umh.es.

J Neurosci ; 37(45): 10773-10782, 2017 11 08.

Article em En | MEDLINE | ID: mdl-29118205

Assuntos

Epigênese Genética/genética; Deficiência Intelectual/etiologia; Deficiência Intelectual/genética; Epigenômica; Humanos

Palavras-chave

Claes-Jensen syndrome; DNA methylation; Kleefstra syndrome; Rett syndrome; Rubinstein-Taybi syndrome; X-linked intellectual disability; histone posttranslational modification; neuroepigenetics; α-thalassemia mental retardation syndrome

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epigênese Genética / Deficiência Intelectual Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

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