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收藏Presence of large deletions in kindreds with autism
Yu, CE; Dawson, G; Munson, J; D'Souza, I; Osterling, J; Estes, A; Leutenegger, AL; Flodman, P; Smith, M; Raskind, WH; Spence, MA; McMahon, W; Wijsman, EM; Schellenberg, GD
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收藏A novel mutation at position+12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto)
Yasuda, M; Takamatsu, J; D'Souza, I; Crowther, RA; Kawamata, T; Hasegawa, M; Hasegawa, H; Spillantini, MG; Tanimukai, S; Poorkaj, P; Varani, L; Varani, G; Iwatsubo, T; Goedert, M; Schellenberg, GD; Tanaka, C
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收藏A mutation in the microtubule-associated protein tau in pallido-nigroluysian degeneration
Yasuda, M; Kawamata, T; Komure, O; Kuno, S; D'Souza, I; Poorkaj, P; Kawai, J; Tanimukai, S; Yamamoto, Y; Hasegawa, H; Sasahara, M; Hazama, F; Schellenberg, GD; Tanaka, C
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收藏Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17
Clark, LN; Poorkaj, P; Wszolek, Z; Geschwind, DH; Nasreddine, ZS; Miller, B; Li, D; Payami, H; Awert, F; Markopoulou, K; Andreadis, A; D'Souza, I; Lee, VMY; Reed, L; Trojanowski, JQ; Zhukareva, V; Bird, T; Schellenberg, G; Wilhelmsen, KC
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