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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