(Q48409394)
Statements
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Screening in ALS and FTD patients reveals 3 novel UBQLN2 mutations outside the PXX domain and a pure FTD phenotype. (English)
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Walter Maetzler
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Ludger Schöls
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Matthis Synofzik
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Torsten Grehl
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Johannes Prudlo
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Jennifer Müller Vom Hagen
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Tobias Haack
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Piret Rebassoo
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Marita Munz
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Saskia Biskup
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11 August 2012
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33
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12
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2949.e13-7
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Identifiers
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