Associated Papers
Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders.
Ortigoza-Escobar JD et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2024
Intellectual disability-associated factor Zbtb11 cooperates with NRF-2/GABP to control mitochondrial function.
Wilson BC et al.
Nature Communications, 2020
Biallelic missense variants in ZBTB11 can cause intellectual disability in humans.
Fattahi Z et al.
Human Molecular Genetics, 2018
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families.
Harripaul R et al.
Molecular Psychiatry, 2018
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