Enigmatic conflict of clinical and molecular diagnosis in Duchenne/Becker muscular dystrophy
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Cited by 17 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. β-Glucans as Dietary Supplement to Improve Locomotion and Mitochondrial Respiration in a Model of Duchenne Muscular Dystrophy;Nutrients;2021-05-12
2. Genome-wide association study to identify potential genetic modifiers in a canine model for Duchenne muscular dystrophy;BMC Genomics;2016-08-22
3. Duchenne muscular dystrophy: Ringo to the rescue?;Neuromuscular Disorders;2016-01
4. Pyrroloquinoline Quinone Resists Denervation-Induced Skeletal Muscle Atrophy by Activating PGC-1α and Integrating Mitochondrial Electron Transport Chain Complexes;PLOS ONE;2015-12-08
5. Revisiting the dystrophin-ATP connection: How half a century of research still implicates mitochondrial dysfunction in Duchenne Muscular Dystrophy aetiology;Medical Hypotheses;2015-12
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