Identification of a Novel Risk Locus for Progressive Supranuclear Palsy by a Pooled Genomewide Scan of 500,288 Single-Nucleotide Polymorphisms

To date, only the H1 MAPT haplotype has been consistently associated with risk of developing the neurodegenerative disease progressive supranuclear palsy (PSP). We hypothesized that additional genetic loci may be involved in conferring risk of PSP that could be identified through a pooling-based gen...

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Main Authors: Melquist, Stacey, Craig, David W., Huentelman, Matthew J., Crook, Richard, Pearson, John V., Baker, Matt, Zismann, Victoria L., Gass, Jennifer, Adamson, Jennifer, Szelinger, Szabolcs, Corneveaux, Jason, Cannon, Ashley, Coon, Keith D., Lincoln, Sarah, Adler, Charles, Tuite, Paul, Calne, Donald B., Bigio, Eileen H., Uitti, Ryan J., Wszolek, Zbigniew K., Golbe, Lawrence I., Caselli, Richard J., Graff-Radford, Neill, Litvan, Irene, Farrer, Matthew J., Dickson, Dennis W., Hutton, Mike, Stephan, Dietrich A.
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society of Human Genetics 2007
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1852701/
https://ncbi.nlm.nih.gov/pubmed/17357082
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