Generation of an induced pluripotent stem cell line (SDQLCHi067-A) from a patient with subcortical band heterotopia harboring a heterozygous mutation in DCX gene
Author:
Funder
Excellent Young Scientists Fund
Natural Science Foundation of Shandong Province
Publisher
Elsevier BV
Reference5 articles.
1. Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia;Haverfield;Eur. J. Hum. Genet.,2009
2. Non-pharmacological treatment options of drug-resistant epilepsy in subcortical band heterotopia: systematic review and illustrative case;Kurzbuch;Childs Nerv. Syst.,2023
3. Novel lissencephaly-associated DCX variants in the C-terminal DCX domain affect microtubule binding and dynamics;Lin;Epilepsia,2022
4. Doublecortin engages the microtubule lattice through a cooperative binding mode involving its C-terminal domain;Rafiei;Elife,2022
5. Domain swap in the C-terminal ubiquitin-like domain of human doublecortin;Rufer;Acta Crystallogr D Struct Biol,2018
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