NMDA receptor gene variations as modifiers in Huntington disease: a replication study

Several candidate modifier genes which, in addition to the pathogenic CAG repeat expansion, influence the age at onset (AO) in Huntington disease (HD) have already been described. The aim of this study was to replicate association of variations in the N-methyl D-aspartate receptor subtype genes GRIN...

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Detalles Bibliográficos
Autores principales: Saft, Carsten, Epplen, Jörg T., Wieczorek, Stefan, Landwehrmeyer, G. Bernhard, Roos, Raymund A.C., de Yebenes, Justo Garcia, Dose, Matthias, Tabrizi, Sarah J, Craufurd, David, Arning, Larissa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Huntington Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3186947/
https://www.ncbi.nlm.nih.gov/pubmed/21989477
http://dx.doi.org/10.1371/currents.RRN1247

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3186947/
https://www.ncbi.nlm.nih.gov/pubmed/21989477
http://dx.doi.org/10.1371/currents.RRN1247

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