Literature DB >> 34537679

Investigating RFC1 expansions in sporadic amyotrophic lateral sclerosis.

Yevgenya Abramzon1, Ramita Dewan2, Andrea Cortese3, Susan Resnick4, Luigi Ferrucci5, Henry Houlden6, Bryan J Traynor7.   

Abstract

A homozygous AAGGG repeat expansion within the RFC1 gene was recently described as a common cause of CANVAS syndrome. We examined 1069 sporadic ALS patients for the presence of this repeat expansion. We did not discover any carriers of the homozygous AAGGG expansion in our ALS cohort, indicating that this form of RFC1 repeat expansions is not a common cause of sporadic ALS. However, our study did identify a novel repeat conformation and further expanded on the highly polymorphic nature of the RFC1 locus.
Copyright © 2021 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  ALS; Motor neuron disorders; RFC1

Mesh:

Substances:

Year:  2021        PMID: 34537679      PMCID: PMC9014296          DOI: 10.1016/j.jns.2021.118061

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   4.553


  25 in total

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4.  A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study.

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Review 5.  Riluzole for amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND).

Authors:  Robert G Miller; J D Mitchell; Dan H Moore
Journal:  Cochrane Database Syst Rev       Date:  2012-03-14

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Authors:  Joseph R Klim; Caroline Vance; Emma L Scotter
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Review 7.  Fragile X spectrum disorders.

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8.  Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia.

Authors:  Roisin Sullivan; Jana Vandrovcova; Mary M Reilly; Andrea Cortese; Roberto Simone; Huma Tariq; Wai Yan Yau; Jack Humphrey; Zane Jaunmuktane; Prasanth Sivakumar; James Polke; Muhammad Ilyas; Eloise Tribollet; Pedro J Tomaselli; Grazia Devigili; Ilaria Callegari; Maurizio Versino; Vincenzo Salpietro; Stephanie Efthymiou; Diego Kaski; Nick W Wood; Nadja S Andrade; Elena Buglo; Adriana Rebelo; Alexander M Rossor; Adolfo Bronstein; Pietro Fratta; Wilson J Marques; Stephan Züchner; Henry Houlden
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9.  Tandem-genotypes: robust detection of tandem repeat expansions from long DNA reads.

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10.  C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease.

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1.  RFC1-Related Disease: Molecular and Clinical Insights.

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  1 in total

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