NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series – further understanding of the relevance of NRXN1 to neurodevelopmental disorders

BACKGROUND: Microdeletions in the NRXN1 gene have been associated with a range of neurodevelopmental disorders, including autism spectrum disorders, schizophrenia, intellectual disability, speech and language delay, epilepsy and hypotonia. RESULTS: In the present study we performed array CGH analysi...

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Detalles Bibliográficos
Autores principales: Curran, Sarah, Ahn, Joo Wook, Grayton, Hannah, Collier, David A, Ogilvie, Caroline Mackie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223877/
https://www.ncbi.nlm.nih.gov/pubmed/25408897
http://dx.doi.org/10.1186/2049-9256-1-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223877/
https://www.ncbi.nlm.nih.gov/pubmed/25408897
http://dx.doi.org/10.1186/2049-9256-1-4

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