Non-coding CGG repeat expansion inLOC642361/NUTM2B-AS1is associated with a phenotype of oculopharyngodistal myopathy
Published 2023 View Full Article
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Title
Non-coding CGG repeat expansion inLOC642361/NUTM2B-AS1is associated with a phenotype of oculopharyngodistal myopathy
Authors
Keywords
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Journal
JOURNAL OF MEDICAL GENETICS
Volume -, Issue -, Pages jmg-2023-109345
Publisher
BMJ
Online
2023-11-04
DOI
10.1136/jmg-2023-109345
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- Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophy
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