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Additional file 2 of Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies

Authors :
Orme, Tatiana
Hernandez, Dena
Ross, Owen
Kun-Rodrigues, Celia
Darwent, Lee
Shepherd, Claire
Parkkinen, Laura
Ansorge, Olaf
Clark, Lorraine
Honig, Lawrence
Marder, Karen
Afina Lemstra
Rogaeva, Ekaterina
George-Hyslop, Peter St.
Londos, Elisabet
Zetterberg, Henrik
Morgan, Kevin
Troakes, Claire
Al-Sarraj, Safa
Tammaryn Lashley
Holton, Janice
Yaroslau Compta
Vivianna Deerlin
Trojanowski, John
Geidy Serrano
Beach, Thomas
Lesage, Suzanne
Galasko, Douglas
Masliah, Eliezer
Santana, Isabel
Pau Pastor
Tienari, Pentti
Myllykangas, Liisa
Oinas, Minna
Revesz, Tamas
Lees, Andrew
Boeve, Brad
Petersen, Ronald
Tanis Ferman
Escott-Price, Valentina
Graff-Radford, Neill
Cairns, Nigel
Morris, John
Pickering-Brown, Stuart
Mann, David
Halliday, Glenda
Stone, David
Dickson, Dennis
Hardy, John
Singleton, Andrew
Guerreiro, Rita
Bras, Jose
Publisher :
figshare

Abstract

Additional file 2: Table S2. Neurodegenerative disease-causing genes and DLB risk genes analysed in this study. Genes known to cause neurodegenerative diseases are presented according to the mode of inheritance of the respective mendelian disease. Genes such as PARK2, FBXO7, SYNJ1, and DNAJC6, among others, are commonly referred to as parkinson’s disease genes, although the clinical and pathological characteristics may be atypical in some cases. FTD/ALS - frontotemporal dementia/Amyotrophic lateral sclerosis, CADASIL - Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, CARASIL - Cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy *Both TMEM230 and DNAJC13 have been hypothesised to be the cause of Parkinson’s disease in the same family.

Subjects

Subjects :
3. Good health

Details

Database :
OpenAIRE
Accession number :
edsair.doi...........542405f7abe61b0a97fabf0263534807