A Case of YY1 ‐Related Isolated Dystonia with Severe Oromandibular Involvement-Reference-Cited by-同舟云学术

A Case of YY1 ‐Related Isolated Dystonia with Severe Oromandibular Involvement

Published:2021-08-19 Issue:11 Volume:36 Page:2705-2706
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Movement Disorders

Author:

Malaquias Maria João¹^ORCID,Damásio Joana¹²,Mendes Alexandre¹,Freixo João Parente²,Magalhães Marina¹

Affiliation:

1. Neurology Department Centro Hospitalar Universitário do Porto Porto Portugal

2. Center for Predictive and Preventive Genetics (CGPP) Institute for Molecular and Cell Biology (IBMC), Instituto de Investigação e Inovação em Saúde (i3S), Universidade do Porto Porto Portugal

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.28771

Reference7 articles.

1. A de novo paradigm for mental retardation

2. YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction

3. A case of YY1 ‐associated syndromic learning disability or Gabriele‐de Vries syndrome with myasthenia gravis

4. Complex movement disorder in a patient with heterozygous YY1 mutation (Gabriele‐de Vries syndrome)

5. A 9‐month‐old Chinese patient with Gabriele‐de Vries syndrome due to novel germline mutation in the YY1 gene

Cited by 6 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. Adult-onset YY1-associated combined dystonia syndrome with infantile nystagmus as a diagnostic clue;Parkinsonism & Related Disorders;2024-07

2. Heterozygous YY1 mutation – A mimicker of SGCE-myoclonus-dystonia;Parkinsonism & Related Disorders;2023-12

3. The expanding genetic landscape of myoclonus-dystonia syndrome: YY1 and ATP1A3 are added to the list;Parkinsonism & Related Disorders;2023-12

4. Transcriptional regulatory network for neuron-glia interactions and its implication for DYT6 dystonia;Dystonia;2023-10-30

5. The apparent paradox of phenotypic diversity and shared mechanisms across dystonia syndromes;Current Opinion in Neurology;2022-07-05