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Wiley, Epilepsia Open, 3(4), p. 397-408, 2019

DOI: 10.1002/epi4.12348

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Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsy

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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