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Pandraud A, Murphy S, Laura M et al. Genetic modifying factors for the common form of CMT1A due to the chromosome 17 duplication and other causes of CMT1 in non-CMT1A patients. F1000Posters 2011, 2:223 (poster)

Genetic modifying factors for the common form of CMT1A due to the chromosome 17 duplication and other causes of CMT1 in non-CMT1A patients

A Pandraud1, S Murphy, M Laura, MM Reilly, H Houlden
Published 14 Apr 2011
Author Affiliations
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Published 14 Apr 2011

Genetic modifying factors for the common form of CMT1A due to the chromosome 17 duplication and other causes of CMT1 in non-CMT1A patients

[version 1; not peer reviewed]

A Pandraud1, S Murphy, M Laura, MM Reilly, H Houlden
Author Affiliations
1 Department of Molecular Neuroscience, MRC Centre for Neuromuscular Disease, ION, University College London, UK
Presented at
UK Neuromuscular Translational Research Conference 2011
Abstract
Competing Interests

No relevant conflicts of interest declared.

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