CPEB alteration and aberrant transcriptome-polyadenylation lead to a treatable SLC19A3 deficiency in Huntington's disease
CPEB 变异和异常转录组多聚腺苷酸化导致亨廷顿氏病中可治疗的 SLC19A3 缺陷
期刊:Science Translational Medicine
影响因子:15.8
doi:10.1126/scitranslmed.abe7104
Sara Picó, Alberto Parras, María Santos-Galindo, Julia Pose-Utrilla, Margarita Castro, Enrique Fraga, Ivó H Hernández, Ainara Elorza, Héctor Anta, Nan Wang, Laura Martí-Sánchez, Eulàlia Belloc, Paula Garcia-Esparcia, Juan J Garrido, Isidro Ferrer, Daniel Macías-García, Pablo Mir, Rafael Artuch, Belé