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Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder.
Li J, Ruskey JA, Arnulf I, Dauvilliers Y, Hu MTM, Högl B, Leblond CS, Zhou S, Ambalavanan A, Ross JP, Bourassa CV, Spiegelman D, Laurent SB, Stefani A, Charley Monaca C, Cochen De Cock V, Boivin M, Ferini-Strambi L, Plazzi G, Antelmi E, Young P, Heidbreder A, Labbe C, Ferman TJ, Dion PA, Fan D, Desautels A, Gagnon JF, Dupré N, Fon EA, Montplaisir JY, Boeve BF, Postuma RB, Rouleau GA, Ross OA, Gan-Or Z. Li J, et al. Mov Disord. 2018 Jul;33(6):1016-1020. doi: 10.1002/mds.27385. Epub 2018 May 14. Mov Disord. 2018. PMID: 29756641 Free article.
TUBA4A may not be a significant genetic factor in Chinese ALS patients.
Li J, He J, Tang L, Chen L, Xu L, Ma Y, Zhang N, Fan D. Li J, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2015;17(1-2):148-50. doi: 10.3109/21678421.2015.1074705. Epub 2015 Oct 14. Amyotroph Lateral Scler Frontotemporal Degener. 2015. PMID: 26465396
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