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.
about
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.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
@zh-hant
name
Identification of the rare com ...... t generalized muscle weakness.
@en
Identification of the rare com ...... t generalized muscle weakness.
@nl
type
label
Identification of the rare com ...... t generalized muscle weakness.
@en
Identification of the rare com ...... t generalized muscle weakness.
@nl
prefLabel
Identification of the rare com ...... t generalized muscle weakness.
@en
Identification of the rare com ...... t generalized muscle weakness.
@nl
P2093
P2860
P356
P1476
Identification of the rare com ...... t generalized muscle weakness.
@en
P2093
Jong-Bin Lee
Jong-Soo Kim
Ki-Young Lee
Seon-Yong Jeong
Shin-Young Yim
Vit-Na Choi
P2860
P2888
P304
P356
10.1038/JHG.2014.87
P577
2014-10-09T00:00:00Z