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Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

artículo científico publicado en 2020

BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder

scientific article published on 30 January 2020

Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders

artículo científico publicado en 2019

Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission

scientific article published on 25 September 2019

Genotype and Phenotype Correlations for TBL1XR1 in Neurodevelopmental Disorders

scientific article published on 10 June 2020

Genotype and phenotype correlations for SHANK3 de novo mutations in neurodevelopmental disorders

artículo científico publicado en 2018

Intergenic sequences harboring potential enhancer elements contribute to Axenfeld-Rieger syndrome by regulating PITX2

artículo científico publicado en 2024

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

scientific article published on 01 October 2020

POGZ de novo missense variants in neuropsychiatric disorders

artículo científico publicado en 2019

Pathogenic missense mutation pattern of forkhead box genes in neurodevelopmental disorders.

artículo científico publicado en 2019

Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD

artículo científico publicado en 2020

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