Modulation at Age of Onset in Tunisian Huntington Disease Patients: Implication of New Modifier Genes

Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder. The causative mutation is an expansion of more than 36 CAG repeats in the first exon of IT15 gene. Many studies have shown that the IT15 interacts with several modifier genes to regulate the age at onset (AO) of HD....

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Detalhes bibliográficos
Main Authors: Hmida-Ben Brahim, Dorra, Chourabi, Marwa, Ben Amor, Sana, Harrabi, Imed, Trabelsi, Saoussen, Haddaji-Mastouri, Marwa, Gribaa, Moez, Sassi, Sihem, Gahbiche, Fatma Ezzahra, Lamouchi, Turkia, Mougou-Zereli, Soumaya, Ben Ammou, Sofiane, Saad, Ali
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4164136/
https://ncbi.nlm.nih.gov/pubmed/25254119
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2014/210418
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