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BMJ Publishing Group, Journal of Medical Genetics, 2(53), p. 127-131, 2015

DOI: 10.1136/jmedgenet-2015-103361

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Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygousOPA1mutation

This paper is available in a repository.
This paper is available in a repository.

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