2013
DOI: 10.9734/bjmmr/2013/2944
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Early-onset CMT1B due to the MPZ mutation c.320A>T associated with collateral inclusion body myopathy and Deafness

Abstract: This work was carried out in collaboration between all authors. Author JF designed the study, performed the evaluation of the data, and wrote the first draft of the manuscript. Author CH was responsible for the nerve and muscle biopsy analysis. Author MAG carried out the genetic studies. All authors read and approved the final manuscript.

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