The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 gene.

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Published in J Neurol on May 05, 2011

Authors

Peter Reilich1, Rita Horvath, Sabine Krause, Nicolai Schramm, Doug M Turnbull, Michael Trenell, Kieren G Hollingsworth, Grainne S Gorman, Volkmar H Hans, Jens Reimann, Andrée MacMillan, Lesley Turner, Annette Schollen, Gregor Witte, Birgit Czermin, Elke Holinski-Feder, Maggie C Walter, Benedikt Schoser, Hanns Lochmüller

Author Affiliations

1: Friedrich-Baur-Institute, Department of Neurology, Ludwig-Maximilians University, Munich, Germany.

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