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Dive into the research topics of 'Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile'. Together they form a unique fingerprint.- Sort by
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Andrea Ciolfi, Aidin Foroutan, Alessandro Capuano, Lucia Pedace, Lorena Travaglini, Simone Pizzi, Marco Andreani, Evelina Miele, Federica Invernizzi, Chiara Reale, Celeste Panteghini, Maria Iascone, Marcello Niceta, Ralitza H. Gavrilova, Laura Schultz-Rogers, Emanuele Agolini, Maria Francesca Bedeschi, Paolo Prontera, Matteo Garibaldi, Serena Galosi
Research output: Contribution to journal › Article › peer-review