Hereditary Motor and Sensory Neuropathy Type VI with Bilateral Middle Cerebellar Peduncle Involvement-Reference-Cited by-同舟云学术

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Hereditary Motor and Sensory Neuropathy Type VI with Bilateral Middle Cerebellar Peduncle Involvement

Published:2014-09-30 Issue:3 Volume:23 Page:266-269
ISSN:1226-2560
Container-title:Experimental Neurobiology
language:en
Short-container-title:Exp Neurobiol

Author:

Oh Jung-Hwan¹,Lee Han Sang²,Cha Dong Min³,Kang Sa-Yoon¹

Affiliation:

1. Department of Neurology, JeJu National University Hospital , JeJu 690-767, Korea

2. Department of Neurology, Seoul National University Hospital, Seoul 110-744, Korea

3. Department of Ophthalmology, JeJu National University Hospital, JeJu 690-767, Korea

Publisher

The Korean Society for Brain and Neural Science

Subject

Cellular and Molecular Neuroscience,Neurology (clinical)

Link

https://synapse.koreamed.org/pdf/10.5607/en.2014.23.3.266

Reference8 articles.

1. Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

2. Peripheral neuropathy in mitochondrial disorders

3. Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations

4. A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies

Cited by 6 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. Mitofusin 2 Variant Presenting With a Phenotype of Multiple System Atrophy of Cerebellar Subtype;Neurology Genetics;2024-02

2. Neuropathy, Hereditary Motor, and Sensory Types VIA and VIB;Genetic Syndromes;2024

3. Hereditary motor and sensory neuropathy type VIA with optic nerve pallor in two sisters with pathologic myopia: a case series and review;Ophthalmic Genetics;2022-09-13

4. Nuclear and Cytoplasmatic Players in Mitochondria-Related CNS Disorders: Chromatin Modifications and Subcellular Trafficking;Biomolecules;2022-04-23

5. A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype;European Journal of Paediatric Neurology;2018-05

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