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Displaying 2 results.

- Journal article
Defects of mutant DNMT1 are linked to a spectrum of neurological disorders
Baets, Jonathan Duan, Xiaohui Wu, Yanhong Smith, Gordon Seeley, William W. Mademan, Inès McGrath, Nicole M. Beadell, Noah C. Khoury, Julie Botuyan, Maria-Victoria Mer, Georges Worrell, Gregory A. Hojo, Kaori DeLeon, Jessica Laura, Matilde Liu, Yo-Tsen Senderek, Jan Weis, Joachim Van den Bergh, Peter[UCL] Merrill, Shana L. Reilly, Mary M. Houlden, Henry Grossman, Murray Scherer, Steven S. De Jonghe, Peter Dyck, Peter J. Klein, Christopher J. (2015) Brain : a journal of neurology — Vol. 138, no. 4, p. 845-861 (2015)
- Journal article
Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentation.
Beijer, Danique Kim, Hong Joo Guo, Lin O'Donovan, Kevin Mademan, Inès Deconinck, Tine Van Schil, Kristof Fare, Charlotte M Drake, Lauren E Ford, Alice F Kochański, Andrzej Kabzińska, Dagmara Dubuisson, Nicolas[UCL] Van den Bergh, Peter[UCL] Voermans, Nicol C Lemmers, Richard Jlf van der Maarel, Silvère M Bonner, Devon Sampson, Jacinda B Wheeler, Matthew T Mehrabyan, Anahit Palmer, Steven De Jonghe, Peter Shorter, James Taylor, J Paul Baets, Jonathan (2021) JCI insight — Vol. 6, no. 14, p. e148363 [1-19] (2021)