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Volume 61, Issue 4
Non-coding CGG repeat expansion in LOC642361/NUTM2B-AS1 is associated with a phenotype of oculopharyngodistal myopathy
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Neurogenetics
Original research
Non-coding CGG repeat expansion in
LOC642361/NUTM2B-AS1
is associated with a phenotype of oculopharyngodistal myopathy
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