Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy-Reference-Cited by-同舟云学术

Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy

Published:2012-02-09 Issue:10 Volume:21 Page:2205-2210
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Winkelmann Juliane,Lin Ling,Schormair Barbara,Kornum Birgitte R.,Faraco Juliette,Plazzi Giuseppe,Melberg Atle,Cornelio Ferdinando,Urban Alexander E.,Pizza Fabio,Poli Francesca,Grubert Fabian,Wieland Thomas,Graf Elisabeth,Hallmayer Joachim,Strom Tim M.,Mignot Emmanuel

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Reference16 articles.

1. Autosomal dominant cerebellar ataxia deafness and narcolepsy;J. Neurol. Sci.,1995

2. Hypocretin deficiency in familial symptomatic narcolepsy;Ann. Neurol.,2001

3. Dnmt1 structure and function;Prog. Mol. Biol. Transl. Sci.,2011

4. Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss;Nat. Genet.,2011

5. Structural insight into maintenance methylation by mouse DNA methyltransferase 1 (Dnmt1);Proc. Natl Acad. Sci. USA,2011

Cited by 219 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The Role of DNMT Methyltransferases and TET Dioxygenases in the Maintenance of the DNA Methylation Level;Biomolecules;2024-09-04

2. The Genetics of Human Sleep and Sleep Disorders;Annual Review of Genomics and Human Genetics;2024-08-27

3. From Environment to Gene Expression: Epigenetic Methylations and One-Carbon Metabolism in Amyotrophic Lateral Sclerosis;Cells;2024-06-03

4. DNA methylation in human diseases;Heliyon;2024-06

5. Mouse Embryonic Stem Cells Require Sustained DNMT1-Mediated DNA Methylation Maintenance for Epigenomic, Genomic and Functional Integrity;2024-05-10