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jhg.2014.87
jhg.2014.87
https://scigraph.springernature.com/pub.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.
P2888
Q48492814-7B066F02-B1F8-4CA9-BBC3-79CE944DF543
P2888
jhg.2014.87
https://scigraph.springernature.com/pub.10.1038/jhg.2014.87