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.2014.120
Published Online: 2015-01-15
Published Print: 2015-03
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Pelin, Katarina
Kiiski, Kirsi
Lehtokari, Vilma-Lotta
Wallgren-Pettersson, Carina
Text and Data Mining valid from 2015-01-15
Article History
First Online: 15 January 2015
Competing interests
: The authors declare no conflict of interest.