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, Shamdeen, Ghiat M., Bogdahn, Ulrich, Schuierer, Gerhard, Topaloglu, Haluk, Aigner, Ludwig, Lochmüller, Hanns and Winkler, Jürgen
(2007)
Novel POMGnT1 mutations define broader phenotypic spectrum of muscle–eye–brain disease.
Neurogenetics 8 (4), pp. 279-288.
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