Systemic Delivery of AAV-Fdxr Mitigates the Phenotypes of Mitochondrial Disorders in Fdxr Mutant Mice-Reference-Cited by-同舟云学术

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Systemic Delivery of AAV-Fdxr Mitigates the Phenotypes of Mitochondrial Disorders in Fdxr Mutant Mice

Published:2020-09 Issue: Volume:18 Page:84-97
ISSN:2329-0501
Container-title:Molecular Therapy - Methods & Clinical Development
language:en
Short-container-title:Molecular Therapy - Methods & Clinical Development

Author:

Yang Li,Slone Jesse,Zou Weiwei,Queme Luis F.,Jankowski Michael P.,Yin Fei,Huang Taosheng

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

Genetics,Molecular Biology,Molecular Medicine

Reference36 articles.

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2. Both human ferredoxins 1 and 2 and ferredoxin reductase are important for iron-sulfur cluster biogenesis;Shi;Biochim. Biophys. Acta,2012

3. Human adrenodoxin reductase: two mRNAs encoded by a single gene on chromosome 17cen----q25 are expressed in steroidogenic tissues;Solish;Proc. Natl. Acad. Sci. USA,1988

4. Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy;Peng;Hum. Mol. Genet.,2017

5. FDXR Mutations Cause Sensorial Neuropathies and Expand the Spectrum of Mitochondrial Fe-S-Synthesis Diseases;Paul;Am. J. Hum. Genet.,2017

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1. Clinical study of ferredoxin-reductase-related mitochondriopathy: Genotype-phenotype correlation and proposal of ancestry-based carrier screening in the Mexican population;Genetics in Medicine Open;2024

2. FDXR-associated disease in a Chinese cohort: Unraveling expanded ocular phenotypes and genetic spectrum;Experimental Eye Research;2023-09

3. FDXR-Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese Population;Genes;2023-04-21

4. Current advances in gene therapy of mitochondrial diseases;Journal of Translational Medicine;2022-12-05

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