Behavioral phenotype in five individuals with de novo mutations within the GRIN2B gene

BACKGROUND: Intellectual disability (ID) is often associated with behavioral problems or disorders. Mutations in the GRIN2B gene (MRD6, MIM613970) have been identified as a common cause of ID (prevalence of 0.5 – 1% in individuals with ID) associated with EEG and behavioral problems. METHODS: We ass...

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Detalles Bibliográficos
Autores principales: Freunscht, Inga, Popp, Bernt, Blank, Rainer, Endele, Sabine, Moog, Ute, Petri, Holger, Prott, Eva-Christina, Reis, Andre, Rübo, Jochen, Zabel, Bernhard, Zenker, Martin, Hebebrand, Johannes, Wieczorek, Dagmar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685602/
https://www.ncbi.nlm.nih.gov/pubmed/23718928
http://dx.doi.org/10.1186/1744-9081-9-20

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685602/
https://www.ncbi.nlm.nih.gov/pubmed/23718928
http://dx.doi.org/10.1186/1744-9081-9-20

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