CrossRef Text and Data Mining
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Single (GCN)11/Ala11 Allele Induces Incomplete Oculopharyngeal Muscular Dystrophy Presenting Atypical Disease Course
Wonjae Sung, Young-Eun Kim, Seung Hyun Kim
Korean J Neuromuscul Disord. 2021;13(1):11-14.   Published online June 30, 2021
DOI: https://doi.org/10.46518/kjnmd.2021.13.1.11

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Single (GCN)11/Ala11 Allele Induces Incomplete Oculopharyngeal Muscular Dystrophy Presenting Atypical Disease Course
Korean Journal of Neuromuscular Disorders. 2021;13(1):11-14   Crossref logo
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Oculopharyngeal Muscular Dystrophy
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Life expectancy of oculopharyngeal muscular dystrophy produced by the (gcn)13/ala 13 expansion mutation in Israels
Journal of the Neurological Sciences. 2015;357:e330   Crossref logo
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Chronic Cough as the Presenting Symptom of Oculopharyngeal Muscular Dystrophy
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Muscular dystrophies and allied disorders V: Facioscapulohumeral, myotonic and oculopharyngeal muscular dystrophy
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OCULOPHARYNGEAL MUSCULAR DYSTROPHY
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Oculopharyngeal Muscular Dystrophy
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Oculopharyngeal muscular dystrophy: a late-onset polyalanine disease
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