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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Syndrome and DCTN1[original query]
Characterization of DCTN1 genetic variability in neurodegeneration.
Neurology 2009 Jun 72 (23): 2024-8.
Vilariño-Güell C, Wider C, Soto-Ortolaza A I, Cobb S A, Kachergus J M, Keeling B H, Dachsel J C, Hulihan M M, Dickson D W, Wszolek Z K, Uitti R J, Graff-Radford N R, Boeve B F, Josephs K A, Miller B, Boylan K B, Gwinn K, Adler C H, Aasly J O, Hentati F, Destée A, Krygowska-Wajs A, Chartier-Harlin M-C, Ross O A, Rademakers R, Farrer M
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
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