Genetic spectrum in a cohort of patients with distal hereditary motor neuropathy-Reference-Cited by-同舟云学术

Genetic spectrum in a cohort of patients with distal hereditary motor neuropathy

Published:2022-03-17 Issue:5 Volume:9 Page:633-643
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann Clin Transl Neurol

Author:

Wu Chengsi¹,Xiang Haijie¹,Chen Ran¹,Zheng Yilei¹,Zhu Min¹²,Chen Shuyun¹,Yu Yanyan¹²,Peng Yun¹²,Yu Yaqing¹,Deng Jianwen³,Zhou Meihong¹,Hong Daojun¹²⁴^ORCID

Affiliation:

1. Department of Neurology The First Affiliated Hospital of Nanchang University Nanchang 330006 China

2. Department of Medical Genetics The First Affiliated Hospital of Nanchang University Nanchang 330006 China

3. Department of Neurology Peking University First Hospital Beijing 100034 China

4. Department of Neurology Peking University People Hospital Beijing 100044 China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangxi Province

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.51543

Reference33 articles.

1. Motor neuropathies and lower motor neuron syndromes

2. Genetic heterogeneity of motor neuropathies

3. Broadening the genetic spectrum of distal hereditary motor neuropathy

4. Next-generation sequencing in Charcot–Marie–Tooth disease: opportunities and challenges

Cited by 14 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. A novel variant of biallelic MME gene associated with autosomal recessive late-onset distal hereditary motor neuropathy in Chinese families;BMC Medical Genomics;2024-09-04

2. A novel mutation in SORD gene associated with distal hereditary motor neuropathies;BMC Medical Genomics;2024-06-24

3. Advances of NOTCH2NLC Repeat Expansions and Associated Diseases: A Bibliometric and Meta-analysis;Molecular Neurobiology;2024-05-06

4. Pathologic changes in neuronal intranuclear inclusion disease are linked to aberrant FUS interaction under hyperosmotic stress;Neurobiology of Disease;2024-01

5. A novel mutation in SORD gene associated with Distal Hereditary Motor Neuropathies;2023-10-11