Exploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathy-Reference-Cited by-同舟云学术

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Exploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathy

Published:2024-04-02 Issue:2 Volume:38 Page:27-34
ISSN:0167-7063
Container-title:Journal of Neurogenetics
language:en
Short-container-title:Journal of Neurogenetics

Author:

Sharma Shivani¹,Mahadevan Anita¹,Narayanappa Gayathri¹,Debnath Monojit²,Govindaraj Periyasamy¹,Shivaram Sumanth³,Seshagiri Doniparthi V.³,Siram Ramesh³,Shroti Akhilesh³,Bindu Parayil S.³,Chickabasaviah Yasha T.¹,Taly Arun B.¹³,Nagappa Madhu³^ORCID

Affiliation:

1. Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bengaluru, India

2. Department of Human Genetics, National Institute of Mental Health and Neurosciences, Bengaluru, India

3. Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India

Funder

Indian Council of Medical Research

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/01677063.2024.2373363

Reference72 articles.

1. Clinical and genetic features of a cohort of patients with MFN2-related neuropathy

2. Subacute peripheral and optic neuropathy syndrome with no evidence of a toxic or nutritional cause

3. Rare Variants in MME , Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies

4. Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and Ireland

5. Epidemic neuropathy in Cuba: Morphological characterization of peripheral nerve lesions in sural nerve biopsies

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