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Intermediate and Expanded HTT Alleles and the Risk for α-Synucleinopathies
Movement Disorders ( IF 8.6 ) Pub Date : 2022-07-19 , DOI: 10.1002/mds.29153
Sergio Pérez-Oliveira 1 , Ignacio Álvarez 2 , Irene Rosas 1 , Manuel Menendez-González 3, 4 , Marta Blázquez-Estrada 3, 4 , Miquel Aguilar 2 , Daniela Corte 5 , Mariateresa Buongiorno 2 , Laura Molina-Porcel 6, 7 , Iban Aldecoa 7, 8 , María J Martí 9, 10 , Pascual Sánchez-Juan 10, 11 , Jon Infante 10, 12 , Isabel González-Aramburu 10, 12 , Pablo García-González 10, 13 , Maitée Rosende-Roca 10, 13 , Mercè Boada 10, 13 , Agustín Ruiz 10, 13 , María Teresa Periñán 10, 14 , Daniel Macías-García 10, 14 , Laura Muñoz-Delgado 10, 14 , Pilar Gómez-Garre 10, 14 , Pablo Mir 10, 14, 15 , Jordi Clarimón 10, 16 , Alberto Lleo 10, 16 , Daniel Alcolea 10, 16 , Beatriz De la Casa-Fages 17, 18 , Israel Duarte 1 , Victoria Álvarez 1, 4 , Pau Pastor 19
Affiliation  

Previous studies suggest a link between CAG repeat number in the HTT gene and non-Huntington neurodegenerative diseases.

中文翻译:

中间和扩展的 HTT 等位基因和 α-突触核蛋白病的风险

先前的研究表明HTT基因中的 CAG 重复数与非亨廷顿神经退行性疾病之间存在联系。
更新日期:2022-07-19
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