Molecular mechanisms underlying nucleotide repeat expansion disorders
Molecular mechanisms underlying nucleotide repeat expansion disorders
About this item
Full title
Author / Creator
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
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Publisher
London: Nature Publishing Group UK
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Scope and Contents
Contents
The human genome contains over one million short tandem repeats. Expansion of a subset of these repeat tracts underlies over fifty human disorders, including common genetic causes of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (
C9orf72
), polyglutamine-associated ataxias and Huntington disease, myotonic dystrophy, and int...
Alternative Titles
Full title
Molecular mechanisms underlying nucleotide repeat expansion disorders
Authors, Artists and Contributors
Author / Creator
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9612635
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9612635
Other Identifiers
ISSN
1471-0072
E-ISSN
1471-0080
DOI
10.1038/s41580-021-00382-6
