Mapping a shared genetic basis for neurodevelopmental disorders

Distinct neurodevelopmental disorders have a common genetic etiology that explains the high degree of comorbidity among these disorders. A recent study sought to identify copy number variants across five neurodevelopmental disorders, and detected an enrichment for chromosome 9p24.3 duplication encom...

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Detalles Bibliográficos
Autores principales: Jensen, Matthew, Girirajan, Santhosh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Highlight
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729609/
https://www.ncbi.nlm.nih.gov/pubmed/29241461
http://dx.doi.org/10.1186/s13073-017-0503-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729609/
https://www.ncbi.nlm.nih.gov/pubmed/29241461
http://dx.doi.org/10.1186/s13073-017-0503-4

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