Novel Machado-Joseph disease-modifying genes and pathways identified by whole-exome sequencing

Funding Information: This work was funded by FEDER - Fundo Europeu de Desenvolvimento Regional funds through the COMPETE 2020 - Operacional Programme for Competitiveness and Internationalisation (POCI), Portugal 2020 , and by Portuguese funds through FCT - Fundação para a Ciência e a Tecnologia / Mi...

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Bibliographic Details
Main Author: Raposo, Mafalda (author)
Other Authors: Bettencourt, Conceição (author), Melo, Ana Rosa Vieira (author), Ferreira, Ana F. (author), Alonso, Isabel (author), Silva, Paulo (author), Vasconcelos, João (author), Kay, Teresa (author), Saraiva-Pereira, Maria Luiza (author), Costa, Marta D. (author), Vilasboas-Campos, Daniela (author), Bettencourt, Bruno Filipe (author), Bruges-Armas, Jácome (author), Houlden, Henry (author), Heutink, Peter (author), Jardim, Laura Bannach (author), Sequeiros, Jorge (author), Maciel, Patrícia (author), Lima, Manuela (author)
Format: article
Language:eng
Published: 2021
Subjects:
Age at onset
Genetic modifier
MJD
Polyglutamine disease
SCA3
Spinocerebellar ataxia
Neurology
Online Access:http://hdl.handle.net/10362/129676
Country:Portugal
Oai:oai:run.unl.pt:10362/129676

Internet

http://hdl.handle.net/10362/129676

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