CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations

Overview of attention for article published in Acta Neuropathologica Communications, November 2020

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Oculopharyngodistal myopathy

Cited by user Rollcloud on 11 Aug 2022

Oculopharyngodistal myopathy is a rare genetic disorder characterized by progressive muscle weakness affecting various parts of the body.

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