DOCK7

Publications

Bai B et al. Novel DOCK7 mutations in a Chinese patient with early infantile epileptic encephalopathy 23. Chinese Medical Journal. 2019;132(5): 600–3. PMID: 30807358.

Haberlandt E et al. Characteristic facial features and cortical blindness distinguish the DOCK7-related epileptic encephalopathy. Mol Genet Genomic Med. 2021 Mar;9(3):e1607. PMID: 33471954.

Nakamuta S et al. Dual role for DOCK7 in tangential migration of interneuron precursors in the postnatal forebrain. J Cell Biol. 2017;216(12):4313–30. PMID: 29089377.

Perrault I et al. Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness. Am J Hum Genet. 2014; 94(6) :891–897. PMID: 24814191.

Turkdogan D et al. A novel truncating mutation of DOCK7 gene with an early-onset non-encephalopathic epilepsy. Seizure. 2019; 66(3):12–4. PMID: 30771731.

Yang YT et al. DOCK7 interacts with TACC3 to regulate interkinetic nuclear migration and cortical neurogenesis. Nat Neurosci. 2012;15(9):1201–10. PMID: 22842144.