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Modeling the human MTM1 p.R69C mutation in murine Mtm1 results in exon 4 skipping and a less severe myotubular myopathy phenotype
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Published in: | Human molecular genetics 2012-02, Vol.21 (4), p.811-825 |
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Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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ISSN: | 0964-6906 1460-2083 |
DOI: | 10.1093/hmg/ddr512 |