Screening in ALS and FTD patients reveals 3 novel UBQLN2 mutations outside the PXX domain and a pure FTD phenotype

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Screening in ALS and FTD patients reveals 3 novel UBQLN2 mutations outside the PXX domain and a pure FTD phenotype

Author: Synofzik, Matthis; Maetzler, Walter; Grehl, Torsten; Prudlo, Johannes; vom Hagen, Jennifer Mueller; Haack, Tobias; Rebassoo, Piret; Munz, Marita; Schoels, Ludger; Biskup, Saskia
Tübinger Autor(en):
Synofzik, Matthis Benjamin
Maetzler, Walter
Prudlo, Johannes
Rebassoo, Piret
Munz, Marita
Biskup, Saskia
Müller vom Hagen, Jennifer Miriam
Schöls, Ludger
Published in: Neurobiology of Aging (2012), Bd. 33, Article 2949.e13
Verlagsangabe: Elsevier Science Inc
Language: English
Full text: http://dx.doi.org/10.1016/j.neurobiolaging.2012.07.002
ISSN: 0197-4580
DDC Classifikation: 610 - Medicine and health
570 - Life sciences; biology
Dokumentart: Artikel
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