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Article

Identification of expanded repeats in NOTCH2NLC in neurodegenerative dementias

24 Jan 2020

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 32081467
DOI: 10.1016/j.neurobiolaging.2020.01.010

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Related research

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Identification of expanded repeats in NOTCH2NLC in neurodegenerative dementiasPMID 32081467Read ↗

NOTCH2NLC-related repeat expansion disorders: an expanding group of neurodegenerative disordersSemantic proximity Read ↗

The expanding biology of the C9orf72 nucleotide repeat expansion in neurodegenerative diseaseSemantic proximity Read ↗

C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairmentSemantic proximity Read ↗

Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related DisordersSemantic proximity Read ↗

Essential phenotypes of NOTCH2NLC-related repeat expansion disorder.Semantic proximity Read ↗

Repeat expansion scanning of the NOTCH2NLC gene in patients with multiple system atrophySemantic proximity Read ↗

NOTCH2NLC-related disorders: the widening spectrum and genotype–phenotype correlationSemantic proximity Read ↗

Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremorSemantic proximity Read ↗

Interrupted CAG expansions in ATXN2 gene expand the genetic spectrum of frontotemporal dementiasSemantic proximity Read ↗

Neuronal intranuclear inclusion disease is genetically heterogeneous.Semantic proximity Read ↗

The Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review.Semantic proximity Read ↗

Short tandem repeat expansions in patients with neurodegenerative dementia.Semantic proximity Read ↗

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