AJOU Open Repository: 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.

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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.

Authors: Yim, SY | Jeong, SY

Citation: Journal of human genetics, 60(3). : 163-164, 2015

Journal Title: Journal of human genetics

ISSN: 1434-51611435-232X

MeSH

DOI: 10.1038/jhg.2014.119

PMID: 25589042

Appears in Collections:: Journal Papers > School of Medicine / Graduate School of Medicine > Physical Medicine & Rehabilitation
Journal Papers > School of Medicine / Graduate School of Medicine > Medical Genetics

Ajou Authors: 임, 신영 | 정, 선용

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