Screening in ALS and FTD patients reveals 3 novel UBQLN2 mutations outside the PXX domain and a pure FTD phenotype
Synofzik, Matthis, Maetzler, Walter, Grehl, Torsten, Prudlo, Johannes, vom Hagen, Jennifer Müller, Haack, Tobias, Rebassoo, Piret, Munz, Marita, Schöls, Ludger, Biskup, Saskia
Published in Neurobiology of aging (01.12.2012)
Published in Neurobiology of aging (01.12.2012)
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