Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene-Reference-Cited by-同舟云学术

Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene

Published:2003-07-07 Issue:4 Volume:54 Page:527-530
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Solano Abelardo,Roig Manuel,Vives-Bauza Cristofol,Hernandez-Peña Jose,Garcia-Arumi Elena,Playan Ana,Lopez-Perez Manuel J.,Andreu Antonio L.,Montoya Julio

Funder

Diputación General de Aragón

Spanish Minister of Health

Spanish Network for Mitochondrial Disorders

Mexican Government

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference13 articles.

1. Lessons from mitochondrial DNA mutations;DiMauro;Semin Cell Dev Biol,2001

2. Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 gene;De Meirleir;Pediatr Neurol,1995

3. Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families;Kirby;Ann Neurol,2000

4. Automatic identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome;Rieder;Nucleic Acids Res,1998

5. Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene;Andreu;Ann Neurol,1999

Cited by 62 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. Clinical overview and phenomenology of movement disorders;Principles and Practice of Movement Disorders;2021

2. Mitochondrial disorders of the OXPHOS system;FEBS Letters;2020-12-18

3. Mitochondrial Dysfunction in Parkinson’s Disease: Focus on Mitochondrial DNA;Biomedicines;2020-12-10

4. Systematic analysis of a mitochondrial disease‐causing ND6 mutation in mitochondrial deficiency;Molecular Genetics & Genomic Medicine;2020-03-12

5. Frequency and association of mitochondrial genetic variants with neurological disorders;Mitochondrion;2019-05