المؤلفون: Dobson-Stone, C, Luty, A, Thompson, EM, Blumbergs, P, Brooks, WS, Short, CL, Field, C, Panegyres, P, Hecker, J, Solski, JA, Blair, I, Fullerton, JM, Halliday, GM, Schofield, PR, Kwok, J, Schofield, Peter

المصدر: urn:ISSN:0001-6322 ; urn:ISSN:1432-0533 ; ACTA Neuropathologica, 125, 4, April 2013, 523-533

مصطلحات موضوعية: Clinical Research, ALS, Frontotemporal Dementia (FTD), Neurodegenerative, Dementia, Neurosciences, Brain Disorders, Acquired Cognitive Impairment, Rare Diseases, Genetics, Alzheimer's Disease Related Dementias (ADRD), Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), 2.1 Biological and endogenous factors, 2 Aetiology, Neurological, Aged, Amyotrophic Lateral Sclerosis, Brain, Chromosomes, Human, Pair 16, DNA-Binding Proteins, Female, Frontotemporal Dementia, Genetic Linkage, Genetic Predisposition to Disease, Haplotypes, Humans, Lod Score, Male

العلاقة: http://purl.org/au-research/grants/nhmrc/APP1062539Test; http://hdl.handle.net/1959.4/unsworks_43868Test; https://doi.org/10.1007/s00401-013-1078-9Test

الإتاحة: https://doi.org/10.1007/s00401-013-1078-9Test
http://hdl.handle.net/1959.4/unsworks_43868Test

المؤلفون: Walters, RG, Jacquemont, S, Valsesia, A, De Smith, AJ, Martinet, D, Andersson, J, Falchi, M, Chen, F, Andrieux, J, Lobbens, S, Delobel, B, Stutzmann, F, El-Sayed Moustafa, JS, Chevre, JC, Lecoeur, C, Vatin, V, Bouquillon, S, Buxton, JL, Boute, O, Holder-Espinasse, M, Cuisset, JM, Lemaitre, MP, Ambresin, AE, Brioschi, A, Gaillard, M, Giusti, V, Fellmann, F, Ferrarini, A, Hadjikhani, N, Campion, D, Guilmatre, A, Goldenberg, A, Calmels, N, Mandel, JL, Le Caignec, C, David, A, Isidor, B, Cordier, MP, Dupuis-Girod, S, Labalme, A, Sanlaville, D, Beri-Dexheimer, M, Jonveaux, P, Leheup, B, Ounap, K, Bochukova, EG, Henning, E, Keogh, J, Ellis, RJ, Macdermot, KD, Van Haelst, MM, Vincent-Delorme, C, Plessis, G, Touraine, R, Philippe, A, Malan, V, Mathieu-Dramard, M, Chiesa, J, Blaumeiser, B, Kooy, RF, Caiazzo, R, Pigeyre, M, Balkau, B, Sladek, R, Bergmann, S, Mooser, V, Waterworth, D, Reymond, A, Vollenweider, P, Waeber, G, Kurg, A, Palta, P, Esko, T, Metspalu, A, Nelis, M, Elliott, P, Hartikainen, AL, McCarthy, MI, Peltonen, L, Carlsson, L, Jacobson, P, Sjostrom, L, Huang, N, Hurles, ME, O'Rahilly, S, Farooqi, IS, Mannik, K, Jarvelin, MR, Pattou, F, Meyre, D, Walley, AJ, Coin, LJ, Blakemore, AI, Froguel, P, Beckmann, JS

المساهمون: Medical Research Council (MRC)

المصدر: 675 ; 671

مصطلحات موضوعية: Science & Technology, Multidisciplinary Sciences, Science & Technology - Other Topics, GENOME-WIDE ASSOCIATION, CIRCULAR BINARY SEGMENTATION, COPY NUMBER VARIATION, FRAMESHIFT MUTATION, RISK LOCI, MICRODELETION, AUTISM, SAMPLE, BIRTH, MC4R, Adolescent, Adult, Age of Onset, Aging, Body Mass Index, Case-Control Studies, Child, Chromosome Deletion, Chromosomes, Human, Pair 16, Cognition Disorders, Cohort Studies, Europe, Female, Genome-Wide Association Study, Heterozygote

العلاقة: Nature; http://hdl.handle.net/10044/1/85527Test; G0600331

الإتاحة: https://doi.org/10.1038/nature08727Test
http://hdl.handle.net/10044/1/85527Test