Large‐scale mitochondrial DNA deletion underlying familial multiple system atrophy of the cerebellar subtype-Reference-Cited by-同舟云学术

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Large‐scale mitochondrial DNA deletion underlying familial multiple system atrophy of the cerebellar subtype

Published:2015-11-23 Issue:2 Volume:4 Page:111-117
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Alsemari Abdulaziz¹,Al‐hindi Hindi Nasser²

Affiliation:

1. Department of Neurosciences King Faisal Specialist Hospital and Research Centre PO box 3354 Riyadh 11211 Saudi Arabia

2. Department of Pathology and Laboratory Medicine King Faisal Specialist Hospital and Research Centre PO box 3354 Riyadh 11211 Saudi Arabia

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.435

Reference37 articles.

1. Mitochondrial diseases

2. Mitochondrial DNA and disease

3. ATAXIA WITH OPHTHALMOPLEGIA OR SENSORY NEUROPATHY IS FREQUENTLY CAUSED BY POLG MUTATIONS

4. Cerebellar ataxia in patients with Leber's hereditary optic neuropathy

5. Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian family

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2. A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome;NAT COMMUN;2022

3. Novel method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome;2022-02-08

4. FTY720-Mitoxy reduces synucleinopathy and neuroinflammation, restores behavior and mitochondria function, and increases GDNF expression in Multiple System Atrophy mouse models;Experimental Neurology;2020-03

5. Cerebral imaging in adult mitochondrial disorders;Journal of the Neurological Sciences;2019-09

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