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Wiley, American Journal of Medical Genetics Part A, 4(158A), p. 772-778, 2012

DOI: 10.1002/ajmg.a.35243

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Recessive RYR1 mutations in a patient with severe congenital nemaline myopathy with ophthalomoplegia identified through massively parallel sequencing

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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