Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity
Author:
Publisher
BMJ
Subject
Psychiatry and Mental health,Clinical Neurology,Surgery
Cited by 48 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. Oculopharyngodistal Myopathy (OPDM);Reference Module in Neuroscience and Biobehavioral Psychology;2024
2. CGG repeat expansion in LOC642361/NUTM2B-AS1 typically presents as oculopharyngodistal myopathy;Journal of Genetics and Genomics;2023-12
3. Choked: A Case Report of Oculopharyngeal Muscular Dystrophy Mimicking Hypothyroidism From the Philippines;Cureus;2023-06-27
4. Recent advances in CGG repeat diseases and a proposal of fragile X-associated tremor/ataxia syndrome, neuronal intranuclear inclusion disease, and oculophryngodistal myopathy (FNOP) spectrum disorder;Journal of Human Genetics;2023-01-20
5. Systemic Complications of Muscular Dystrophies;Current Clinical Neurology;2023
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