Associated Papers
Characteristic facial features and cortical blindness distinguish the DOCK7-related epileptic encephalopathy.
Haberlandt E et al.
Molecular Genetics & Genomic Medicine, 2021
Novel DOCK7 mutations in a Chinese patient with early infantile epileptic encephalopathy 23.
Bai B et al.
Chinese Medical Journal, 2019
In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery.
Oliver KL et al.
Neurology. Genetics, 2016
27066588 (PubMed )
Supplement: supp_2.1.e51_table_e-2.xlsx › table_e-2
Novel Genes of Early-Onset Epileptic Encephalopathies: From Genotype to Phenotypes.
Mastrangelo M
Pediatric Neurology, 2015
Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness.
Perrault I et al.
American Journal of Human Genetics, 2014
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