Abstract
Long-read Sequencing Identifies GGC Repeat Expansions in NOTCH2NLC as the Cause of Neuronal Intranuclear Inclusion Disease (2832)
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https://doi.org/10.1212/wnl.94.15_supplement.2832
Journal: Neurology | Publication Date: Apr 14, 2020 |
Long-read Sequencing Identifies GGC Repeat Expansions in NOTCH2NLC as the Cause of Neuronal Intranuclear Inclusion Disease (2832)
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