Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia
Nature Genetics2012Vol. 44(10), pp. 1080–1083
Citations Over TimeTop 10% of 2012 papers
M. Zimoń, Jonathan Baets, Leonardo Almeida‐Souza, Els De Vriendt, J. Nikodinović, Yeşim Parman, Esra Battaloğlu, Zeliha Matur, Velina Guergueltcheva, Ivailo Tournev, Michaela Auer‐Grumbach, Peter De Rijk, Britt‐Sabina Petersen, Thomas Müller, Erik Fransen, Philip Van Damme, Wolfgang N. Löscher, Nina Barišić, Zoran D. Mitrović, Stefano C. Previtali, Haluk Topaloğlu, Günther Bernert, Ana Beleza‐Meireles, S. Todorović, Dušanka Savić‐Pavićević, Boryana Ishpekova, Silvia Lechner, Kristien Peeters, Tinne Ooms, Angelika F. Hahn, Stephan Züchner, Vincent Timmerman, Patrick Van Dijck, Vedrana Milić Rašić, Andreas Janecke, Peter De Jonghe, Albena Jordanova
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