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|a Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies
|c 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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|a Aus: Orphanet Journal of Rare Diseases, 9 (2014), Nr. 121. pp. 1-13. ISSN 1750-1172
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