An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14
Titel:
An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14
Auteur:
Rafehi, Haloom Read, Justin Szmulewicz, David J. Davies, Kayli C. Snell, Penny Fearnley, Liam G. Scott, Liam Thomsen, Mirja Gillies, Greta Pope, Kate Bennett, Mark F. Munro, Jacob E. Ngo, Kathie J. Chen, Luke Wallis, Mathew J. Butler, Ernest G. Kumar, Kishore R. Wu, Kathy HC. Tomlinson, Susan E. Tisch, Stephen Malhotra, Abhishek Lee-Archer, Matthew Dolzhenko, Egor Eberle, Michael A. Roberts, Leslie J. Fogel, Brent L. Brüggemann, Norbert Lohmann, Katja Delatycki, Martin B. Bahlo, Melanie Lockhart, Paul J.