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Elsevier, Genetics in Medicine, 2(19), p. 144-156, 2017

DOI: 10.1038/gim.2016.86

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EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causality

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

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Abstract

Peer reviewed