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Autor:
Mukherjee, Oditi, Pastor, Pau, Cairns, Nigel J, Chakraverty, Sumi, Kauwe, John S.K., Shears, Shantia, Behrens, Maria I, Budde, John, Hinricks, Anthony L, Norton, Joanne, Levitch, Denise, Taylor-Reinwald, Lisa, Gitcho, Michael, Tu, P-H, Tenenholz Grinberg, Lea, Liščić, Rajka, Armendariz, Javier, Morris, John C, Goate, Alison
Objective Familial autosomal dominant frontotemporal dementia with ubiquitin-positive, tau-negative inclusions in the brain linked to 17q21-22 recently has been reported to carry null mutations in the progranulin gene (PGRN). Hereditary dysphasic dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::30e1911b8458adf689adf62d87316bb8
https://www.bib.irb.hr/255602
https://www.bib.irb.hr/255602