Associated Papers
Functional and Epigenomic Consequences of DNMT1 Variants in Inherited Neurological Disorders.
Yuan JH et al.
International Journal of Molecular Sciences, 2026
Cerebellar Ataxia as a Common Clinical Presentation Associated with DNMT1 p.Y511H and a Review of the Literature.
Kikuchi JK et al.
Journal of Molecular Neuroscience : Mn, 2021
Expanded genetic insight and clinical experience of DNMT1-complex disorder.
Bi H et al.
Neurology. Genetics, 2020
DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism.
Maresca A et al.
Human Molecular Genetics, 2020
Modifiers and Readers of DNA Modifications and Their Impact on Genome Structure, Expression, and Stability in Disease.
Ludwig AK et al.
Frontiers in Genetics, 2016
A novel de novo exon 21 DNMT1 mutation causes cerebellar ataxia, deafness, and narcolepsy in a Brazilian patient.
Pedroso JL et al.
Sleep, 2013
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