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Update on genetics of essential tremor
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Jiménez-Jiménez, F.J., Alonso-Navarro, H., García-Martín, E., Lorenzo-Betancor, O., Pastor, P., Agúndez, J.A. Update on genetics of essential tremor. Acta Neurol. Scand. doi:10.1111/ane.12148.
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Acta Neurol. Scand.
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Jiménez-Jiménez, F.J.1
Alonso-Navarro, H.2
García-Martín, E.3
Lorenzo-Betancor, O.4
Pastor, P.5
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Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
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Kwiatkowski T.J., Bosco D.A., Leclerc A.L., Tamrazian E., Vanderburg C.R., Russ C., Davis A., Gilchrist J., Kasarskis E.J., Munsat T., Valdmanis P., Rouleau G.A., Hosler B.A., Cortelli P., de Jong P.J., Yoshinaga Y., Haines J.L., Pericak-Vance M.A., Yan J., Ticozzi N., Siddique T., McKenna-Yasek D., Sapp P.C., Horvitz H.R., Landers J.E., Brown R.H. Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 2009, 323:1205-1208.
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79960307713
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Lack of association of LINGO1 rs9652490 and rs11856808 SNPs with familial essential tremor
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Lorenzo-Betancor O., García-Martín E., Cervantes S., Agúndez J.A., Jiménez-Jiménez F.J., Alonso-Navarro H., Luengo A., Coria F., Lorenzo E., Irigoyen J., Pastor P. Lack of association of LINGO1 rs9652490 and rs11856808 SNPs with familial essential tremor. Eur. J. Neurol. 2011, 18:1085-1089.
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Lorenzo-Betancor, O.1
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Jiménez-Jiménez, F.J.5
Alonso-Navarro, H.6
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Lorenzo, E.9
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77951230101
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How common is the most common adult movement disorder? Update on the worldwide prevalence of essential tremor
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Louis E.D., Ferreira J.J. How common is the most common adult movement disorder? Update on the worldwide prevalence of essential tremor. Mov. Disord. 2010, 25:534-541.
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Louis, E.D.1
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Exome sequencing identifies FUS mutations as a cause of essential tremor
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Merner N.D., Girard S.L., Catoire H., Bourassa C.V., Belzil V.V., Rivière J.B., Hince P., Levert A., Dionne-Laporte A., Spiegelman D., Noreau A., Diab S., Szuto A., Fournier H., Raelson J., Belouchi M., Panisset M., Cossette P., Dupré N., Bernard G., Chouinard S., Dion P.A., Rouleau G.A. Exome sequencing identifies FUS mutations as a cause of essential tremor. Am. J. Hum. Genet. 2012, 91:313-319.
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84873894614
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Genetic analysis of the FUS/TLS gene in essential tremor
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Parmalee N., Mirzozoda K., Kisselev S., Merner N., Dion P., Rouleau G., Clark L., Louis E.D. Genetic analysis of the FUS/TLS gene in essential tremor. Eur. J. Neurol. 2013, 20:534-539.
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7
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61349106502
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Variant in the sequence of the LINGO1 gene confers risk of essential tremor
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Stefansson H., Steinberg S., Petursson H., Gustafsson O., Gudjonsdottir I.H., Jonsdottir G.A., Palsson S.T., Jonsson T., Saemundsdottir J., Bjornsdottir G., Böttcher Y., Thorlacius T., Haubenberger D., Zimprich A., Auff E., Hotzy C., Testa C.M., Miyatake L.A., Rosen A.R., Kristleifsson K., Rye D., Asmus F., Schöls L., Dichgans M., Jakobsson F., Benedikz J., Thorsteinsdottir U., Gulcher J., Kong A., Stefansson K. Variant in the sequence of the LINGO1 gene confers risk of essential tremor. Nat. Genet. 2009, 41:277-279.
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8
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84866096968
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Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor
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Thier S., Lorenz D., Nothnagel M., Poremba C., Papengut F., Appenzeller S., Paschen S., Hofschulte F., Hussl A.C., Hering S., Poewe W., Asmus F., Gasser T., Schöls L., Christensen K., Nebel A., Schreiber S., Klebe S., Deuschl G., Kuhlenbäumer G. Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor. Neurology 2012, 79:243-248.
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Thier, S.1
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Kuhlenbäumer, G.20
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9
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61349162349
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Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
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Vance C., Rogelj B., Hortobágyi T., De Vos K.J., Nishimura A.L., Sreedharan J., Hu X., Smith B., Ruddy D., Wright P., Ganesalingam J., Williams K.L., Tripathi V., Al-Saraj S., Al-Chalabi A., Leigh P.N., Blair I.P., Nicholson G., deBelleroche J., Gallo J.M., Miller C.C., Shaw C.E. Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science 2009, 323:1208-1211.
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Vance, C.1
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Hu, X.7
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