Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia-Reference-Cited by-同舟云学术

Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia

Published:2013-09-20 Issue:3 Volume:23 Page:749-754
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Dols-Icardo O.,Garcia-Redondo A.,Rojas-Garcia R.,Sanchez-Valle R.,Noguera A.,Gomez-Tortosa E.,Pastor P.,Hernandez I.,Esteban-Perez J.,Suarez-Calvet M.,Anton-Aguirre S.,Amer G.,Ortega-Cubero S.,Blesa R.,Fortea J.,Alcolea D.,Capdevila A.,Antonell A.,Llado A.,Munoz-Blanco J. L.,Mora J. S.,Galan-Davila L.,Rodriguez De Rivera F. J.,Lleo A.,Clarimon J.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/23/3/749/14141922/ddt460.pdf

Reference18 articles.

1. Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS

2. A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

3. 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

4. Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population

5. Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisation

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