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A newly identified Thr99fsX110 mutation in the PMP22 gene associated with an atypical phenotype of the hereditary neuropathy with liability to pressure palsies

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Description scientific article published on 15 October 2009
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author: Izabela Moszyńska  Dagmara Kabzińska  Elena Sinkiewicz-Darol  Andrzej Kochański 

Publication date October 15, 2009
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