A reply to 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
Crossref DOI link: https://doi.org/10.1038/jhg.2014.119
Published Online: 2015-01-15
Published Print: 2015-03
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Yim, Shin-Young
Jeong, Seon-Yong
Text and Data Mining valid from 2015-01-15
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First Online: 15 January 2015