Genetic Modification of Huntington Disease Acts Early in the Prediagnosis Phase

Age at onset of Huntington disease, an inherited neurodegenerative disorder, is influenced by the size of the disease-causing CAG trinucleotide repeat expansion in HTT and by genetic modifier loci on chromosomes 8 and 15. Stratifying by modifier genotype, we have examined putamen volume, total motor...

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Publicat a:Am J Hum Genet
Autors principals: Long, Jeffrey D., Lee, Jong-Min, Aylward, Elizabeth H., Gillis, Tammy, Mysore, Jayalakshmi Srinidhi, Abu Elneel, Kawther, Chao, Michael J., Paulsen, Jane S., MacDonald, Marcy E., Gusella, James F.
Format: Artigo
Idioma:Inglês
Publicat: Elsevier 2018
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6128248/
https://ncbi.nlm.nih.gov/pubmed/30122542
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2018.07.017
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