Identification of genomic deletions spanning the PCDH19 gene in two unrelated girls with intellectual disability and seizures.
about
Tenogenic modulating insider factor: Systematic assessment on the functions of tenomodulin geneGenome-Wide Detection of CNVs and Their Association with Meat Tenderness in Nelore CattleIntellectual disability and autism spectrum disorders: causal genes and molecular mechanisms.Tetraspanin 6: A novel regulator of hippocampal synaptic transmission and long term plasticity.PCDH19-related infantile epileptic encephalopathy: an unusual X-linked inheritance disorder.Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders.Male patients affected by mosaic PCDH19 mutations: five new cases.Regulation of neural circuit formation by protocadherins.The clinical spectrum of female epilepsy patients with PCDH19 mutations in a Chinese population.Pathophysiology of Trans-Synaptic Adhesion Molecules: Implications for Epilepsy
P2860
Q26748847-8E359DD6-46E6-4514-B418-6910B69FBA86Q27339172-276BCA30-4B8E-4769-8EAD-36199272424FQ34289505-98EDEEC4-04F2-4F5F-8346-A2B0193C072EQ36282851-34F6747D-776E-4EDC-B4F5-F978897EDE6BQ37977871-0DE7A0F4-1396-45DC-84C9-A25021F931C1Q38075436-EF7FD957-A310-4D02-BF52-B68BD1C9EBEAQ38698169-DDDE765A-3334-4BD2-B4D1-C30E5D93FD99Q38718127-71594E19-5A2F-4E64-A54A-7A02D6FEE335Q40092559-DA922A1F-6D3F-4BDB-AA42-C03F690ED0CCQ57299992-AC795048-BF8D-4612-86D6-11A378B3BEB2
P2860
Identification of genomic deletions spanning the PCDH19 gene in two unrelated girls with intellectual disability and seizures.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh-hant
name
Identification of genomic dele ...... ctual disability and seizures.
@en
Identification of genomic dele ...... ctual disability and seizures.
@nl
type
label
Identification of genomic dele ...... ctual disability and seizures.
@en
Identification of genomic dele ...... ctual disability and seizures.
@nl
prefLabel
Identification of genomic dele ...... ctual disability and seizures.
@en
Identification of genomic dele ...... ctual disability and seizures.
@nl
P2093
P2860
P1433
P1476
Identification of genomic dele ...... ctual disability and seizures.
@en
P2093
A K Vincent
B A Minassian
J B Vincent
P2860
P304
P356
10.1111/J.1399-0004.2011.01812.X
P577
2011-12-13T00:00:00Z