Journal of Neurogenetics, Volume 38, Issue 2 (2024)

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Journal of Neurogenetics, Volume 38, Issue 2 (2024)

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Original Research Articles

Article
Exploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathy
Shivani Sharma, Anita Mahadevan, Gayathri Narayanappa, Monojit Debnath, Periyasamy Govindaraj, Sumanth Shivaram, Doniparthi V. Seshagiri, Ramesh Siram, Akhilesh Shroti, Parayil S. Bindu, Yasha T. Chickabasaviah, Arun B. Taly & Madhu Nagappa
Pages: 27-34
Published online: 08 Jul 2024
AbstractforExploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathy | Full Text | References | PDF (808.7 KB) | EPUB | Supplemental
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Article
SORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause
Annabelle Arlt, Esra Akova-Öztürk, Anja Schirmacher, Bernhard Schlüter, Stephan Rust, Gerd Meyer zu Hörste, Heinz Wiendl & Sarah Wiethoff
Pages: 35-40
Published online: 08 Jul 2024
AbstractforSORDD: mutation frequency and phenotype in predominantly axonal Charcot-Marie-Tooth disease of undefined genetic cause | Full Text | References | PDF (909.4 KB) | EPUB
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Open Access

Brief Report

Brief Report
Carbamazepine responsive episodic dystonia and hallucination due to pyruvate dehydrogenase E2 (DLAT) gene mutation
Jasmine Policherla, Fatema J. Serajee, Salman Rashid & A. H. M. Mahbubul Huq
Pages: 41-45
Published online: 15 Jul 2024
AbstractforCarbamazepine responsive episodic dystonia and hallucination due to pyruvate dehydrogenase E2 (DLAT) gene mutation | Full Text | References | PDF (654.4 KB) | EPUB
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