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TMEM106B is a genetic modifier of frontotemporal lobar dege..:
Gallagher, Michael D
;
Suh, Eunran
;
Grossman, Murray
...
qt6978s69z. , 2014
Link:
https://escholarship.org/uc/item/6978s69z
RT Journal T1
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt6978s69z&Exemplar=1&LAN=DE A1 Gallagher, Michael D A1 Suh, Eunran A1 Grossman, Murray A1 Elman, Lauren A1 McCluskey, Leo A1 Van Swieten, John C A1 Al-Sarraj, Safa A1 Neumann, Manuela A1 Gelpi, Ellen A1 Ghetti, Bernardino A1 Rohrer, Jonathan D A1 Halliday, Glenda A1 Van Broeckhoven, Christine A1 Seilhean, Danielle A1 Shaw, Pamela J A1 Frosch, Matthew P A1 Alafuzoff, Irina A1 Antonell, Anna A1 Bogdanovic, Nenad A1 Brooks, William A1 Cairns, Nigel J A1 Cooper-Knock, Johnathan A1 Cotman, Carl A1 Cras, Patrick A1 Cruts, Marc A1 De Deyn, Peter P A1 DeCarli, Charles A1 Dobson-Stone, Carol A1 Engelborghs, Sebastiaan A1 Fox, Nick A1 Galasko, Douglas A1 Gearing, Marla A1 Gijselinck, Ilse A1 Grafman, Jordan A1 Hartikainen, Päivi A1 Hatanpaa, Kimmo J A1 Highley, J Robin A1 Hodges, John A1 Hulette, Christine A1 Ince, Paul G A1 Jin, Lee-Way A1 Kirby, Janine A1 Kofler, Julia A1 Kril, Jillian A1 Kwok, John BJ A1 Levey, Allan A1 Lieberman, Andrew A1 Llado, Albert A1 Martin, Jean-Jacques A1 Masliah, Eliezer A1 McDermott, Christopher J A1 McKee, Ann A1 McLean, Catriona A1 Mead, Simon A1 Miller, Carol A A1 Miller, Josh A1 Munoz, David G A1 Murrell, Jill A1 Paulson, Henry A1 Piguet, Olivier A1 Rossor, Martin A1 Sanchez-Valle, Raquel A1 Sano, Mary A1 Schneider, Julie A1 Silbert, Lisa C A1 Spina, Salvatore A1 van der Zee, Julie A1 Van Langenhove, Tim A1 Warren, Jason A1 Wharton, Stephen B A1 White, Charles L A1 Woltjer, Randall L A1 Trojanowski, John Q A1 Lee, Virginia MY A1 Van Deerlin, Vivianna A1 Chen-Plotkin, Alice S PB eScholarship, University of California YR 2014 K1 Humans K1 Amyotrophic Lateral Sclerosis K1 Genetic Predisposition to Disease K1 Intercellular Signaling Peptides and Proteins K1 Proteins K1 Membrane Proteins K1 Nerve Tissue Proteins K1 Cohort Studies K1 Age Factors K1 Age of Onset K1 DNA Repeat Expansion K1 Genotype K1 Heterozygote K1 Polymorphism K1 Single Nucleotide K1 Alleles K1 Adult K1 Aged K1 80 and over K1 Middle Aged K1 Female K1 Male K1 Frontotemporal Lobar Degeneration K1 C9orf72 Protein K1 Progranulins K1 Rare Diseases K1 Aging K1 Neurosciences K1 Alzheimer's Disease Related Dementias (ADRD) K1 Brain Disorders K1 Neurodegenerative K1 Prevention K1 Genetics K1 Dementia K1 Frontotemporal Dementia (FTD) K1 Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD) K1 Acquired Cognitive Impairment K1 Aetiology K1 2.1 Biological and endogenous factors K1 Neurological K1 TMEM106B K1 C9orf72 K1 Frontotemporal dementia K1 Genetic modifier K1 Clinical Sciences K1 Neurology & Neurosurgery JF qt6978s69z LK http://dx.doi.org/https://escholarship.org/uc/item/6978s69z DO https://escholarship.org/uc/item/6978s69z SF ELIB - SuUB Bremen
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