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Gene networks associated with non-syndromic intellectual disability

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Journal of Neurogenetics 32 (1) 6 (2018)
DOI: 10.1080/01677063.2017.1404058
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Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1

Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, et al.
Nature Genetics 45 (7) 825 (2013)
DOI: 10.1038/ng.2646
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