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MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical features

The microtubule-associated protein tau (MAPT) H1 haplotype is the strongest genetic risk factor for corticobasal degeneration (CBD). However, the specific H1 subhaplotype association is not well defined, and it is not clear whether any MAPT haplotypes influence severity of tau pathology or clinical...

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Detalhes bibliográficos
Publicado no:Acta Neuropathol Commun
Main Authors: Valentino, Rebecca R., Koga, Shunsuke, Walton, Ronald L., Soto-Beasley, Alexandra I., Kouri, Naomi, DeTure, Michael A., Murray, Melissa E., Johnson, Patrick W., Petersen, Ronald C., Boeve, Bradley F., Uitti, Ryan J., Wszolek, Zbigniew K., Dickson, Dennis W., Ross, Owen A., Heckman, Michael G.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7720600/
https://ncbi.nlm.nih.gov/pubmed/33287913
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-020-01097-z
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