Subclinical peripheral neuropathy is common in neuronal intranuclear inclusion disease with dominant encephalopathy-Reference-Cited by-同舟云学术

Subclinical peripheral neuropathy is common in neuronal intranuclear inclusion disease with dominant encephalopathy

Published:2022-11 Issue:2 Volume:30 Page:527-537
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Euro J of Neurology

Author:

Hong Daojun¹²^ORCID,Wang Hui³⁴,Zhu Min¹²,Peng Yun¹²,Huang Pengcheng¹,Zheng Yilei¹,Yu Meng³⁴,Meng Lingchao³⁴,Li Fan³⁴,Yu Jiaxi³⁴,Zhou Meihong¹,Deng Jianwen³⁴,Wang Zhaoxia³⁴,Yuan Yun³⁴^ORCID

Affiliation:

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

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

3. Department of Neurology Peking University First Hospital Beijing China

4. Beijing Key Laboratory of Neurovascular Disease Discovery Beijing China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ene.15606

Reference30 articles.

1. Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease

2. Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion disease

3. Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders

4. Long-read sequencing identified repeat expansions in the 5′UTR of the NOTCH2NLC gene from Chinese patients with neuronal intranuclear inclusion disease

5. Neuronal intranuclear inclusion disease in patients with adult-onset non-vascular leukoencephalopathy

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