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P40 Autosomal dominant centronuclear myopathy caused by a heterozygous stop-mutation in BIN1 – A case report
P40 Autosomal dominant centronuclear myopathy caused by a heterozygous stop-mutation in BIN1 – A case report
2020
T. Dyong
Katja Eggermann
Ingo Kurth
Joachim Weis
B. Gess
Jörg B. Schulz
M.F. Dohrn
Keywords:
Autosomal dominant centronuclear myopathy
Psychology
Genetics
Mutation
Neuroscience
Correction
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