Multiple mitochondrial DNA deletions in monozygotic twins with OPMD-Reference-Cited by-同舟云学术

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Multiple mitochondrial DNA deletions in monozygotic twins with OPMD

Published:2008-01-01 Issue:1 Volume:79 Page:68-71
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:Journal of Neurology, Neurosurgery & Psychiatry

Author:

Muqit M M K,Larner A J,Sweeney M G,Sewry C,Stinton V J,Davis M B,Healy D G,Payne S J,Chotai K,Wood N W,Lane R J M

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Cited by 11 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. Emerging and established biomarkers of oculopharyngeal muscular dystrophy;Neuromuscular Disorders;2023-11

2. Mitochondrial myopathy with a unique presentation of facial and bulbar muscle weakness caused by single large scale mitochondrial DNA deletion;Clinical Neuropathology;2021-09-01

3. Differential phenotypic expression of a novel PDHA1 mutation in a female monozygotic twin pair;Human Genetics;2019-10-31

4. Toxic myopathy with multiple deletions in mitochondrial DNA associated with long‐term use of oral anti‐viral drugs for hepatitis B: A case study;Neuropathology;2019-03-07

5. Human Stakeholders and the Use of Animals in Drug Development;Business and Society Review;2018-03

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