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JHG.2014.87
JHG.2014.87
http://dx.doi.org/10.1038/JHG.2014.87
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.
P356
Q48492814-833AE779-232A-476E-8DB4-7F012206EF20
P356
JHG.2014.87
http://dx.doi.org/10.1038/JHG.2014.87