Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies

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Bibliographic Details
Main Authors: Semmler, Anna-Lena (Author) , Müller, Oliver J. (Author)
Format: Article (Journal) Book/Monograph
Language:English
Published: London BioMed Central 2016
Online Access:Resolving-System, kostenfrei, Volltext: http://nbn-resolving.de/urn:nbn:de:bsz:16-heidok-197584
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Author Notes:Anna-Lena Semmler, Sabrina Sacconi, J. Elisa Bach, Claus Liebe, Jan Bürmann, Rudolf A. Kley, Andreas Ferbert, Roland Anderheiden, Peter Van den Bergh, Jean-Jacques Martin, Peter De Jonghe, Eva Neuen-Jacob, Oliver Müller, Marcus Deschauer, Markus Bergmann, J. Michael Schröder, Matthias Vorgerd, Jörg B. Schulz, Joachim Weis, Wolfram Kress and Kristl G. Claeys
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Item Description:Gesehen am 16.02.2016
Aus: Orphanet Journal of Rare Diseases, 9 (2014), Nr. 121. pp. 1-13. ISSN 1750-1172
Physical Description:Online Resource