Additional file 2 of Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile
- Andrea Ciolfi (4021622)
- Aidin Foroutan (11263717)
- Alessandro Capuano (7554794)
- Lucia Pedace (8263269)
- Lorena Travaglini (7554791)
- Simone Pizzi (8263266)
- Marco Andreani (4683250)
- Evelina Miele (1307871)
- Federica Invernizzi (3519104)
- Chiara Reale (11263720)
- Celeste Panteghini (11108867)
- Maria Iascone (3597656)
- Marcello Niceta (4021628)
- Ralitza H. Gavrilova (11263723)
- Laura Schultz-Rogers (11263726)
- Emanuele Agolini (9577349)
- Maria Francesca Bedeschi (4526644)
- Paolo Prontera (11263729)
- Matteo Garibaldi (6177266)
- Serena Galosi (8982170)
- Vincenzo Leuzzi (500280)
- Paola Soliveri (7154510)
- Rory J. Olson (11263732)
- Giovanna S. Zorzi (11263735)
- Barbara M. Garavaglia (11263738)
- Marco Tartaglia (11263741)
- Bekim Sadikovic (56562)
Publication date
August 2021
DOIAbstract
Additional file 2: Figure S2. Volcano plot of differences in the methylation status of individual probes between patients carrying pathogenic KMT2B variants and controls versus statistical significance (-log p-value) of individual probes. Red dots represent selected, significant differentially methylated probes (DMPs) in Pt. 1-8. Positive and negative mean methylation difference show hypermethylation and hypomethylation, respectively
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