Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Atrophy and DCTN1[original query] |
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Mutation analysis of genes within the dynactin complex in a cohort of hereditary peripheral neuropathies. Clinical genetics 2015 Dec . Tey Shelisa, Ahmad-Annuar Azlina, Drew Alexander P, Shahrizaila Nortina, Nicholson Garth A, Kennerson Marina |
DCTN1 p.K56R in progressive supranuclear palsy. Parkinsonism & related disorders 2016 Apr . Gustavsson Emil K, Trinh Joanne, Guella Ilaria, Szu-Tu Chelsea, Khinda Jaskaran, Lin Chin-Hsien, Wu Ruey-Meei, Stoessl Jon, Appel-Cresswell Silke, McKeown Martin, Rajput Alex, Rajput Ali H, Petersen Maria Skaalum, Jeon Beom S, Aasly Jan O, Farrer Matthew |
Neuropathological findings in a South Korean patient with Perry syndrome. Clinical neuropathology 2019 12 39 (2): 80-85. Chung Eun Joo, Kim Sang Jin, Kim Eun-Joo, Ahn Jae Woo, Huh Gi Yeong, Cho Hwa Jin, Cairns Nigel |
DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB. Neurobiology of aging 2020 Apr . Procopio Radha, Gagliardi Monica, D'Amelio Marco, Brighina Laura, Nicoletti Giuseppe, Morelli Maurizio, Bonapace Giuseppe, Quattrone Aldo, Annesi Graz |
Genetic Spectrum and Clinical Heterogeneity of Chinese Frontotemporal Dementia Patients: Data from PUMCH Dementia Cohort. Journal of Alzheimer's disease : JAD 2022 Aug . Dong Liling, Wang Jie, Liu Caiyan, Li Jie, Mao Chenhui, Huang Xinying, Chu Shanshan, Peng Bin, Cui Liying, Gao Ji |
[Genetic distribution in Chinese patients with hereditary peripheral neuropathy]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2022 10 54 (5): 874-883. Liu X X, Duan X H, Zhang S, Sun A P, Zhang Y S, Fan D |
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