A de novo missense mutation in SLC12A5 found in a compound heterozygote patient with epilepsy of infancy with migrating focal seizures.
about
A de novo missense mutation in SLC12A5 found in a compound heterozygote patient with epilepsy of infancy with migrating focal seizures.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年学术文章
@wuu
2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
@zh-sg
2017年學術文章
@yue
2017年學術文章
@zh
2017年學術文章
@zh-hant
name
A de novo missense mutation in ...... with migrating focal seizures.
@en
A de novo missense mutation in ...... with migrating focal seizures.
@nl
type
label
A de novo missense mutation in ...... with migrating focal seizures.
@en
A de novo missense mutation in ...... with migrating focal seizures.
@nl
prefLabel
A de novo missense mutation in ...... with migrating focal seizures.
@en
A de novo missense mutation in ...... with migrating focal seizures.
@nl
P2093
P2860
P356
P1433
P1476
A de novo missense mutation in ...... with migrating focal seizures
@en
P2093
P2860
P304
P356
10.1111/CGE.13049
P577
2017-09-15T00:00:00Z