1p34.3 deletion involving GRIK3: Further clinical implication of GRIK family glutamate receptors in the pathogenesis of developmental delay.
about
A gain-of-function mutation in the GRIK2 gene causes neurodevelopmental deficitsIonotropic GABA and Glutamate Receptor Mutations and Human Neurologic Diseases.de novo interstitial deletions at the 11q23.3-q24.2 regionCommon genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood.Prenatal diagnosis of 1p34.3 interstitial microdeletion by aCGH in a fetus with jaw bone abnormalities.
P2860
1p34.3 deletion involving GRIK3: Further clinical implication of GRIK family glutamate receptors in the pathogenesis of developmental delay.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
1p34.3 deletion involving GRIK ...... enesis of developmental delay.
@en
1p34.3 deletion involving GRIK ...... enesis of developmental delay.
@nl
type
label
1p34.3 deletion involving GRIK ...... enesis of developmental delay.
@en
1p34.3 deletion involving GRIK ...... enesis of developmental delay.
@nl
prefLabel
1p34.3 deletion involving GRIK ...... enesis of developmental delay.
@en
1p34.3 deletion involving GRIK ...... enesis of developmental delay.
@nl
P2093
P2860
P356
P1476
1p34.3 deletion involving GRIK ...... enesis of developmental delay.
@en
P2093
Chiharu Torii
Kenjiro Kosaki
Noriko Hashida
Rika Kosaki
Takao Takahashi
Toshiki Takenouchi
P2860
P304
P356
10.1002/AJMG.A.36240
P407
P577
2013-11-25T00:00:00Z