Genotyping FOXG1 Mutations in Patients with Clinical Evidence of the FOXG1 Syndrome.
about
Striatal neurodevelopment is dysregulated in purine metabolism deficiency and impacts DARPP-32, BDNF/TrkB expression and signaling: new insights on the molecular and cellular basis of Lesch-Nyhan Syndrome.Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay.FOXG1 Mutation is a Low-Incidence Genetic Cause in Atypical Rett Syndrome.
P2860
Genotyping FOXG1 Mutations in Patients with Clinical Evidence of the FOXG1 Syndrome.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Genotyping FOXG1 Mutations in Patients with Clinical Evidence of the FOXG1 Syndrome.
@ast
Genotyping FOXG1 Mutations in Patients with Clinical Evidence of the FOXG1 Syndrome.
@en
type
label
Genotyping FOXG1 Mutations in Patients with Clinical Evidence of the FOXG1 Syndrome.
@ast
Genotyping FOXG1 Mutations in Patients with Clinical Evidence of the FOXG1 Syndrome.
@en
prefLabel
Genotyping FOXG1 Mutations in Patients with Clinical Evidence of the FOXG1 Syndrome.
@ast
Genotyping FOXG1 Mutations in Patients with Clinical Evidence of the FOXG1 Syndrome.
@en
P2093
P2860
P356
P1476
Genotyping FOXG1 Mutations in Patients with Clinical Evidence of the FOXG1 Syndrome.
@en
P2093
J V Warner
M G Williams
P2860
P304
P356
10.1159/000345845
P577
2012-12-12T00:00:00Z