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ArticleJournal of human genetics2015

A commentary on identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weakness.

Katarina Pelin et al.PubMed ↗Publisher ↗

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1 paper cites it

2015

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A commentary on identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weakness. | OpenQuestion