The frequency of the C9orf72 expansion in a Brazilian population

Author:

Cintra Vívian PedigoneORCID,Bonadia Luciana Cardoso,Andrade Helen Maia T.,de Albuquerque Milena,Eusébio Mayara Ferreira,de Oliveira Daniel Sabino,Claudino Rinaldo,Gonçalves Marcus Vinicius Magno,Teixeira Antônio Lúcio,de Godoy Rousseff Prado Laura,de Souza Leonardo Cruz,Dourado Mario Emilio Teixeira,Oliveira Acary Souza Bulle,Tumas Vitor,França Marcondes C.,Marques Wilson

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference24 articles.

1. Characterization of an FTLD-PDB family with the coexistence of SQSTM1 mutation and hexanucleotide (G(4)C(2)) repeat expansion in C9orf72 gene;Almeida;Neurobiol. Aging,2016

2. Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72;Boeve;Brain,2012

3. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis;Brooks;Amyotroph. Lateral Scler. Other Mot. Neuron Disord.,2000

4. Genetic analysis of patients with familial and sporadic amyotrophic lateral sclerosis in a Brazilian Research Center;Chadi;Amyotroph. Lateral Scler. Frontotemporal Degener.,2016

5. Rapidly progressive frontotemporal dementia and bulbar amyotrophic lateral sclerosis in Portuguese patients with C9orf72 mutation;Chester;Amyotroph. Lateral Scler. Frontotemporal Degener.,2013

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