Review of Phenotypic Heterogeneity of Neuronal Intranuclear Inclusion Disease and <i>NOTCH2NLC</i> -Related GGC Repeat Expansion Disorders-Reference-Cited by-同舟云学术

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Review of Phenotypic Heterogeneity of Neuronal Intranuclear Inclusion Disease and NOTCH2NLC -Related GGC Repeat Expansion Disorders

Published:2024-04 Issue:2 Volume:10 Page:
ISSN:2376-7839
Container-title:Neurology Genetics
language:en
Short-container-title:Neurol Genet

Author:

Zhang Tao¹^ORCID,Bao Lei¹^ORCID,Chen Hao¹^ORCID

Affiliation:

1. From the Department of Neurology (T.Z., L.B., H.C.), the Affiliated Hospital of Xuzhou Medical University; and Department of Neurology (L.B.), Xuzhou Medical University, China.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Link

https://www.neurology.org/doi/pdfdirect/10.1212/NXG.0000000000200132

Reference56 articles.

1. Clinical Features and Classification of Neuronal Intranuclear Inclusion Disease

2. Clinical features of NOTCH2NLC-related neuronal intranuclear inclusion disease

3. The Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review

4. Re‐defining the clinicopathological spectrum of neuronal intranuclear inclusion disease

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

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1. The evolving spectrum of complex inherited neuropathies;Current Opinion in Neurology;2024-07-31

2. STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci;2024-05-21

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