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Korean Neurological Association, Journal of Clinical Neurology (Seoul, Korea), 2(11), p. 183, 2015

DOI: 10.3988/jcn.2015.11.2.183

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Molecular Genetic Diagnosis of a Bethlem Myopathy Family with an Autosomal-DominantCOL6A1Mutation, as Evidenced by Exome Sequencing

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Data provided by SHERPA/RoMEO