Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Kierra P. Hobdy"'
Autor:
Skylar E. Davis, Anna K. Cook, Justin A. Hall, Yuliya Voskobiynyk, Nancy V. Carullo, Nicholas R. Boyle, Ahmad R. Hakim, Kristian M. Anderson, Kierra P. Hobdy, Derian A. Pugh, Charles F. Murchison, Laura J. McMeekin, Micah Simmons, Katherine A. Margolies, Rita M. Cowell, Alissa L. Nana, Salvatore Spina, Lea T. Grinberg, Bruce L. Miller, William W. Seeley, Andrew E. Arrant
Publikováno v:
Acta Neuropathologica Communications, Vol 11, Iss 1, Pp 1-19 (2023)
Abstract Loss of function progranulin (GRN) mutations are a major autosomal dominant cause of frontotemporal dementia (FTD). Patients with FTD due to GRN mutations (FTD-GRN) develop frontotemporal lobar degeneration with TDP-43 pathology type A (FTLD
Externí odkaz:
https://doaj.org/article/cb7d9e8149f4472c81b6d7612826356c
Autor:
Skylar E. Davis, Anna K. Cook, Yuliya Voskobiynyk, Nancy VN Carullo, Ahmad R. Hakim, Kristian M. Anderson, Kierra P. Hobdy, Derian A Pugh, Charles F Murchison, Laura J. McMeekin, Micah S. Simmons, Rita M. Cowell, Alissa Nana Li, Salvatore Spina, Lea Tenenholz Grinberg, Bruce L. Miller, William W. Seeley, Andrew E. Arrant
Publikováno v:
Alzheimer's & Dementia. 18